Paracetamol - FDA Approved Drugs
Paracetamol
FDA approved drug product records including application numbers, product numbers, active ingredients, dosage forms, strengths, approval dates and regulatory status.
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FDA Approved Drug Records (739 records)
Drug Name
VICODIN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 85667
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACEPHEN
Product Number
1
Dosage Form
-
Strength
120MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 18060
Product No.: 1
Product
Dosage Form: -
Strength: 120MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACEPHEN
Product Number
2
Dosage Form
-
Strength
650MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 18060
Product No.: 2
Product
Dosage Form: -
Strength: 650MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACEPHEN
Product Number
3
Dosage Form
-
Strength
325MG
Approval Date
Dec 18, 1986
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 18060
Product No.: 3
Product
Dosage Form: -
Strength: 325MG
Approval Date
Dec 18, 1986
Regulatory Status
Discontinued
Drug Name
ACEPHEN
Product Number
1
Dosage Form
-
Strength
120MG
Approval Date
Mar 27, 1992
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 72218
Product No.: 1
Product
Dosage Form: -
Strength: 120MG
Approval Date
Mar 27, 1992
Regulatory Status
Discontinued
Drug Name
ACEPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Mar 27, 1992
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 72237
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Mar 27, 1992
Regulatory Status
Discontinued
Drug Name
ACEPHEN
Product Number
1
Dosage Form
-
Strength
325MG
Approval Date
Mar 27, 1992
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 72344
Product No.: 1
Product
Dosage Form: -
Strength: 325MG
Approval Date
Mar 27, 1992
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
120MG
Approval Date
May 12, 1987
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 71010
Product No.: 1
Product
Dosage Form: -
Strength: 120MG
Approval Date
May 12, 1987
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
May 12, 1987
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 71011
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
May 12, 1987
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/50ML (10MG/ML)
Approval Date
Feb 18, 2021
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 204957
Product No.: 1
Product
Dosage Form: -
Strength: 500MG/50ML (10MG/ML)
Approval Date
Feb 18, 2021
Regulatory Status
RX
Drug Name
ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Feb 18, 2021
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 204957
Product No.: 2
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Feb 18, 2021
Regulatory Status
RX
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/VIAL
Approval Date
Jan 15, 2021
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 206610
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/VIAL
Approval Date
Jan 15, 2021
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
May 31, 2018
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 207035
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
May 31, 2018
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
May 03, 2023
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 215403
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
May 03, 2023
Regulatory Status
RX
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Oct 25, 2022
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 216467
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Oct 25, 2022
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Jul 27, 2022
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 216617
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Jul 27, 2022
Regulatory Status
RX
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Dec 05, 2025
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 219096
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Dec 05, 2025
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Apr 26, 1996
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40119
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Apr 26, 1996
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
May 29, 2008
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40779
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
May 29, 2008
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jul 16, 1992
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 81249
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jul 16, 1992
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jul 16, 1992
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 81250
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jul 16, 1992
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 83871
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 83872
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 84360
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
325MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85217
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85288
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
325MG;45MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85363
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;45MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
325MG;15MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85364
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;15MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85365
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85607
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85676
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 86549
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87006
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87141
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Oct 18, 1985
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89183
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Oct 18, 1985
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Oct 18, 1985
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89184
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Oct 18, 1985
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Oct 18, 1985
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89185
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Oct 18, 1985
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
May 19, 1986
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89253
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
May 19, 1986
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
May 19, 1986
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89254
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
May 19, 1986
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Oct 27, 1992
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89450
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Oct 27, 1992
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Mar 03, 1987
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89478
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Mar 03, 1987
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Mar 03, 1987
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89479
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Mar 03, 1987
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Mar 03, 1987
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89480
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Mar 03, 1987
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Mar 03, 1987
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89481
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Mar 03, 1987
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Mar 03, 1987
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89482
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Mar 03, 1987
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Mar 03, 1987
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89483
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Mar 03, 1987
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Sep 30, 1988
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89805
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Sep 30, 1988
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Sep 30, 1988
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89828
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Sep 30, 1988
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Sep 30, 1988
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89990
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Sep 30, 1988
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Dec 28, 1994
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89997
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Dec 28, 1994
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Dec 28, 1994
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89998
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Dec 28, 1994
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Dec 28, 1994
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89999
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Dec 28, 1994
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Nov 10, 2011
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 91238
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Nov 10, 2011
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Jun 27, 2019
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 211610
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Jun 27, 2019
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jun 27, 2019
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 211610
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jun 27, 2019
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
3
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jun 27, 2019
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 211610
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jun 27, 2019
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND HYDROCODONE BITARTRATE
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Mar 27, 1985
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 88898
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Mar 27, 1985
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Feb 28, 2023
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 214836
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Feb 28, 2023
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Jul 13, 2023
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 216592
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Jul 13, 2023
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Aug 23, 2024
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 218247
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Aug 23, 2024
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Apr 26, 2024
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 218311
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Apr 26, 2024
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Dec 11, 2025
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 220126
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Dec 11, 2025
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN, CAFFEINE AND DIHYDROCODEINE BITARTRATE
Product Number
1
Dosage Form
-
Strength
325MG;30MG;16MG
Approval Date
Sep 30, 2016
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Identifiers
Application No.: 204209
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;30MG;16MG
Approval Date
Sep 30, 2016
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE
Product Number
1
Dosage Form
-
Strength
356.4MG;30MG;16MG
Approval Date
Apr 03, 2007
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Identifiers
Application No.: 40688
Product No.: 1
Product
Dosage Form: -
Strength: 356.4MG;30MG;16MG
Approval Date
Apr 03, 2007
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE
Product Number
1
Dosage Form
-
Strength
712.8MG;60MG;32MG
Approval Date
Apr 03, 2007
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Identifiers
Application No.: 40701
Product No.: 1
Product
Dosage Form: -
Strength: 712.8MG;60MG;32MG
Approval Date
Apr 03, 2007
Regulatory Status
Discontinued
Drug Name
ALLZITAL
Product Number
1
Dosage Form
-
Strength
325MG;25MG
Approval Date
Dec 04, 2015
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 203484
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;25MG
Approval Date
Dec 04, 2015
Regulatory Status
RX
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Oct 05, 1988
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 89568
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Oct 05, 1988
Regulatory Status
Discontinued
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;50MG
Approval Date
Dec 04, 2015
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 203484
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Dec 04, 2015
Regulatory Status
RX
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;50MG
Approval Date
Dec 27, 2017
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 207313
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG
Approval Date
Dec 27, 2017
Regulatory Status
RX
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;50MG
Approval Date
Nov 22, 2019
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 213115
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG
Approval Date
Nov 22, 2019
Regulatory Status
RX
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;50MG
Approval Date
Apr 07, 2022
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 214088
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG
Approval Date
Apr 07, 2022
Regulatory Status
RX
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;25MG
Approval Date
Apr 07, 2022
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 214088
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;25MG
Approval Date
Apr 07, 2022
Regulatory Status
RX
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;50MG
Approval Date
Apr 07, 2022
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 214088
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Apr 07, 2022
Regulatory Status
RX
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Jan 18, 2024
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 214291
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Jan 18, 2024
Regulatory Status
RX
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;50MG
Approval Date
Feb 01, 2024
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 214305
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG
Approval Date
Feb 01, 2024
Regulatory Status
RX
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;50MG
Approval Date
Aug 16, 2022
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 214955
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG
Approval Date
Aug 16, 2022
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG/15ML;50MG/15ML;40MG/15ML
Approval Date
Jan 31, 2003
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40387
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/15ML;50MG/15ML;40MG/15ML
Approval Date
Jan 31, 2003
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Aug 27, 2003
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40511
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Aug 27, 2003
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jul 29, 2005
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40601
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jul 29, 2005
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Dec 01, 2008
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40864
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Dec 01, 2008
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Nov 13, 1984
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 87629
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Nov 13, 1984
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Dec 05, 1984
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 88825
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Dec 05, 1984
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Mar 17, 1986
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 89007
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Mar 17, 1986
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Sep 13, 2012
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 200243
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Sep 13, 2012
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Oct 28, 2016
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 207118
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Oct 28, 2016
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Dec 17, 2019
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 210817
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Dec 17, 2019
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Sep 26, 2018
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 211106
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Sep 26, 2018
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Dec 17, 2019
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 212082
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Dec 17, 2019
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Dec 17, 2019
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 212083
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Dec 17, 2019
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Apr 08, 2020
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 213321
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Apr 08, 2020
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Aug 13, 2021
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 214087
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Aug 13, 2021
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
2
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Aug 13, 2021
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 214087
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Aug 13, 2021
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jan 18, 2024
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 214287
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jan 18, 2024
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Feb 08, 2024
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 214288
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Feb 08, 2024
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Nov 17, 2021
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 215047
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Nov 17, 2021
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Mar 12, 2024
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 216376
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Mar 12, 2024
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN, CAFFEINE AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG;30MG
Approval Date
Apr 22, 2002
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 75929
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG;30MG
Approval Date
Apr 22, 2002
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN, CAFFEINE AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG;30MG
Approval Date
Jul 08, 2020
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 204649
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG;30MG
Approval Date
Jul 08, 2020
Regulatory Status
Discontinued
Drug Name
BUTALBITAL; ACETAMINOPHEN; CAFFEINE; CODEINE
Product Number
2
Dosage Form
-
Strength
40MG/30MG
Approval Date
-
Active Ingredient
BUTALBITAL; ACETAMINOPHEN; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 76528
Product No.: 2
Product
Dosage Form: -
Strength: 40MG/30MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CAPITAL AND CODEINE
Product Number
1
Dosage Form
-
Strength
325MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 83643
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
CO-GESIC
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Mar 02, 1988
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89360
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Mar 02, 1988
Regulatory Status
Discontinued
Drug Name
CODEINE, ASPIRIN, APAP FORMULA NO. 2
Product Number
1
Dosage Form
-
Strength
150MG;180MG;15MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; ASPIRIN; CODEINE PHOSPHATE
Identifiers
Application No.: 85640
Product No.: 1
Product
Dosage Form: -
Strength: 150MG;180MG;15MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
CODEINE, ASPIRIN, APAP FORMULA NO. 3
Product Number
1
Dosage Form
-
Strength
150MG;180MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; ASPIRIN; CODEINE PHOSPHATE
Identifiers
Application No.: 85639
Product No.: 1
Product
Dosage Form: -
Strength: 150MG;180MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
CODEINE, ASPIRIN, APAP FORMULA NO. 4
Product Number
1
Dosage Form
-
Strength
150MG;180MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; ASPIRIN; CODEINE PHOSPHATE
Identifiers
Application No.: 85638
Product No.: 1
Product
Dosage Form: -
Strength: 150MG;180MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
COMBOGESIC
Product Number
1
Dosage Form
-
Strength
325MG;97.5MG
Approval Date
Mar 01, 2023
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 209471
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;97.5MG
Approval Date
Mar 01, 2023
Regulatory Status
RX
Drug Name
DARVOCET A500
Product Number
1
Dosage Form
-
Strength
500MG;100MG
Approval Date
Sep 10, 2003
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 76429
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;100MG
Approval Date
Sep 10, 2003
Regulatory Status
Discontinued
Drug Name
DARVOCET-N 100
Product Number
2
Dosage Form
-
Strength
650MG;100MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 17122
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
DARVOCET-N 50
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 17122
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
DOLENE AP-65
Product Number
1
Dosage Form
-
Strength
650MG;65MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE
Identifiers
Application No.: 85100
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;65MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
HY-PHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
May 03, 1982
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 87677
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
May 03, 1982
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Apr 28, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40248
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Apr 28, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;10MG
Approval Date
Apr 28, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40248
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Apr 28, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;10MG
Approval Date
May 31, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40355
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
May 31, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jan 22, 2003
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40432
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jan 22, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/15ML;7.5MG/15ML
Approval Date
Sep 25, 2003
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40482
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/15ML;7.5MG/15ML
Approval Date
Sep 25, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jan 19, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40655
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jan 19, 2006
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jan 19, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40656
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jan 19, 2006
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Jan 19, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40658
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Jan 19, 2006
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Mar 24, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40658
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Mar 24, 2006
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Jun 23, 2004
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40658
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Jun 23, 2004
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Aug 25, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40729
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Aug 25, 2006
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Aug 25, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40736
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Aug 25, 2006
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;10MG
Approval Date
Aug 25, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40746
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Aug 25, 2006
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
May 10, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40746
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
May 10, 2016
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Aug 25, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40748
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Aug 25, 2006
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Aug 25, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40754
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Aug 25, 2006
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;10MG
Approval Date
Aug 25, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40757
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Aug 25, 2006
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Aug 28, 2006
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40769
Product No.: 1
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Aug 28, 2006
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;10MG
Approval Date
Feb 23, 2007
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40813
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
Feb 23, 2007
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/15ML;7.5MG/15ML
Approval Date
Jul 19, 2011
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40894
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/15ML;7.5MG/15ML
Approval Date
Jul 19, 2011
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jun 12, 1987
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89554
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jun 12, 1987
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Jan 24, 2011
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90415
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Jan 24, 2011
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Jan 24, 2011
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90415
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Jan 24, 2011
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Jan 24, 2011
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90415
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Jan 24, 2011
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/15ML;7.5MG/15ML
Approval Date
Jan 25, 2012
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 200343
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/15ML;7.5MG/15ML
Approval Date
Jan 25, 2012
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jun 15, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202935
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jun 15, 2016
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jun 15, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202935
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jun 15, 2016
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jun 15, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202935
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jun 15, 2016
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Jul 05, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 205001
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Jul 05, 2016
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Jul 05, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 205001
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Jul 05, 2016
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Jul 05, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 205001
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Jul 05, 2016
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Jun 23, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206869
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Jun 23, 2017
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Jun 20, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207171
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Jun 20, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Jun 20, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207171
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Jun 20, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Jun 20, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207171
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Jun 20, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jun 22, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207172
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jun 22, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jun 22, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207172
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jun 22, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jun 22, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207172
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jun 22, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Oct 29, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207509
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Oct 29, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Oct 29, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207509
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Oct 29, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Oct 29, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207509
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Oct 29, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Jun 21, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209036
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Jun 21, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Jun 21, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209036
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Jun 21, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Jun 21, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209036
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Jun 21, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jun 21, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209037
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jun 21, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jun 21, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209037
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jun 21, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jun 21, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209037
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jun 21, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Nov 07, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211487
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Nov 07, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Nov 07, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211487
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Nov 07, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Nov 07, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211487
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Nov 07, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Nov 07, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211487
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Nov 07, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Feb 07, 2020
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211690
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Feb 07, 2020
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Feb 07, 2020
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211690
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Feb 07, 2020
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Feb 07, 2020
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211690
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Feb 07, 2020
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jan 03, 2020
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211729
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jan 03, 2020
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jan 03, 2020
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211729
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jan 03, 2020
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jan 03, 2020
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211729
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jan 03, 2020
Regulatory Status
RX
Drug Name
INJECTAPAP
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
Mar 07, 1986
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 17785
Product No.: 1
Product
Dosage Form: -
Strength: 100MG/ML
Approval Date
Mar 07, 1986
Regulatory Status
Discontinued
Drug Name
MEDIGESIC PLUS
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jan 14, 1986
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 89115
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jan 14, 1986
Regulatory Status
Discontinued
Drug Name
NORCET
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
May 15, 1986
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 88871
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
May 15, 1986
Regulatory Status
Discontinued
Drug Name
OFIRMEV
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Nov 02, 2010
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 22450
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Nov 02, 2010
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jul 30, 1996
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40105
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jul 30, 1996
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Nov 27, 2007
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40777
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Nov 27, 2007
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;10MG
Approval Date
Nov 27, 2007
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40778
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Nov 27, 2007
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jun 27, 2014
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40778
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jun 27, 2014
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Nov 27, 2007
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40789
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Nov 27, 2007
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG;10MG
Approval Date
Nov 27, 2007
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40789
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Nov 27, 2007
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
May 04, 1989
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 89994
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
May 04, 1989
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Oct 20, 2008
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90177
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Oct 20, 2008
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Oct 20, 2008
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90177
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Oct 20, 2008
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Oct 20, 2008
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90177
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Oct 20, 2008
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Oct 20, 2008
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90177
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Oct 20, 2008
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
5
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Oct 20, 2008
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90177
Product No.: 5
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Oct 20, 2008
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
6
Dosage Form
-
Strength
650MG;10MG
Approval Date
Oct 20, 2008
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90177
Product No.: 6
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Oct 20, 2008
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Jul 11, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90733
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Jul 11, 2013
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jul 11, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90734
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jul 11, 2013
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jul 11, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90734
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jul 11, 2013
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/5ML;5MG/5ML
Approval Date
Aug 26, 2021
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201448
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/5ML;5MG/5ML
Approval Date
Aug 26, 2021
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Sep 25, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207333
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Sep 25, 2017
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;10MG
Approval Date
Sep 25, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207333
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Sep 25, 2017
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Mar 22, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207419
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Mar 22, 2017
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Mar 22, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207419
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Mar 22, 2017
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Mar 22, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207419
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Mar 22, 2017
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Mar 22, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207419
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Mar 22, 2017
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Dec 13, 2016
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207574
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Dec 13, 2016
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Aug 15, 2019
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207834
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Aug 15, 2019
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Aug 15, 2019
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207834
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Aug 15, 2019
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Aug 15, 2019
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207834
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Aug 15, 2019
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Feb 09, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 210644
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Feb 09, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Feb 09, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 210644
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Feb 09, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Feb 09, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 210644
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Feb 09, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Feb 09, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 210644
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Feb 09, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/5ML;5MG/5ML
Approval Date
Dec 31, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 211499
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/5ML;5MG/5ML
Approval Date
Dec 31, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Oct 31, 2019
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 211708
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Oct 31, 2019
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Oct 31, 2019
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 211708
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Oct 31, 2019
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Oct 31, 2019
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 211708
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Oct 31, 2019
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Oct 31, 2019
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 211708
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Oct 31, 2019
Regulatory Status
RX
Drug Name
OXYCODONE HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/5ML;5MG/5ML
Approval Date
Dec 18, 2014
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 203573
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/5ML;5MG/5ML
Approval Date
Dec 18, 2014
Regulatory Status
Discontinued
Drug Name
PAPA-DEINE #3
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Mar 20, 1984
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88037
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Mar 20, 1984
Regulatory Status
Discontinued
Drug Name
PAPA-DEINE #4
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Mar 20, 1984
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88715
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Mar 20, 1984
Regulatory Status
Discontinued
Drug Name
PERCOCET
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Jun 25, 1999
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40330
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Jun 25, 1999
Regulatory Status
RX
Drug Name
PERCOCET
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jun 25, 1999
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40330
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jun 25, 1999
Regulatory Status
RX
Drug Name
PERCOCET
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Nov 23, 2001
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40330
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Nov 23, 2001
Regulatory Status
RX
Drug Name
PERCOCET
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Nov 23, 2001
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40330
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Nov 23, 2001
Regulatory Status
RX
Drug Name
PERCOCET
Product Number
2
Dosage Form
-
Strength
325MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 85106
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
PHENAPHEN W/ CODEINE NO. 2
Product Number
1
Dosage Form
-
Strength
325MG;15MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 84444
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;15MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
PHENAPHEN W/ CODEINE NO. 3
Product Number
1
Dosage Form
-
Strength
325MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 84445
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
PHENAPHEN W/ CODEINE NO. 4
Product Number
1
Dosage Form
-
Strength
325MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 84446
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
PHENAPHEN-650 W/ CODEINE
Product Number
1
Dosage Form
-
Strength
650MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85856
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Jan 06, 1987
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 71319
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Jan 06, 1987
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
May 13, 1988
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 72105
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
May 13, 1988
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
May 13, 1988
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 72106
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
May 13, 1988
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;100MG
Approval Date
May 07, 2004
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 76743
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;100MG
Approval Date
May 07, 2004
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;100MG
Approval Date
Jun 28, 2004
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 76750
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;100MG
Approval Date
Jun 28, 2004
Regulatory Status
Discontinued
Drug Name
SEDAPAP
Product Number
1
Dosage Form
-
Strength
650MG;50MG
Approval Date
Oct 17, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 88944
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;50MG
Approval Date
Oct 17, 1985
Regulatory Status
Discontinued
Drug Name
SYNALGOS-DC-A
Product Number
1
Dosage Form
-
Strength
356.4MG;30MG;16MG
Approval Date
May 14, 1986
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Identifiers
Application No.: 89166
Product No.: 1
Product
Dosage Form: -
Strength: 356.4MG;30MG;16MG
Approval Date
May 14, 1986
Regulatory Status
Discontinued
Drug Name
TALACEN
Product Number
1
Dosage Form
-
Strength
650MG;EQ 25MG BASE
Approval Date
Sep 23, 1982
Active Ingredient
ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE
Identifiers
Application No.: 18458
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;EQ 25MG BASE
Approval Date
Sep 23, 1982
Regulatory Status
Discontinued
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
Apr 21, 2005
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 76475
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
Apr 21, 2005
Regulatory Status
Discontinued
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
Jul 26, 2006
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 76914
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
Jul 26, 2006
Regulatory Status
Discontinued
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
Sep 26, 2008
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 77858
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
Sep 26, 2008
Regulatory Status
RX
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
Apr 07, 2014
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 78778
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
Apr 07, 2014
Regulatory Status
Discontinued
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
Sep 06, 2012
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 90460
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
Sep 06, 2012
Regulatory Status
RX
Drug Name
TRIAPRIN
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Jul 02, 1987
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 89268
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Jul 02, 1987
Regulatory Status
Discontinued
Drug Name
TYCOLET
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Aug 27, 1986
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89385
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Aug 27, 1986
Regulatory Status
Discontinued
Drug Name
TYLENOL
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 17756
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL
Product Number
2
Dosage Form
-
Strength
120MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 17756
Product No.: 2
Product
Dosage Form: -
Strength: 120MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Jun 08, 1994
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 19872
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Jun 08, 1994
Regulatory Status
OTC
Drug Name
TYLENOL
Product Number
2
Dosage Form
-
Strength
650MG
Approval Date
Jan 11, 2001
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 19872
Product No.: 2
Product
Dosage Form: -
Strength: 650MG
Approval Date
Jan 11, 2001
Regulatory Status
OTC
Drug Name
TYLENOL W/ CODEINE
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85056
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL W/ CODEINE
Product Number
2
Dosage Form
-
Strength
325MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85056
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL W/ CODEINE
Product Number
3
Dosage Form
-
Strength
325MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85056
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL W/ CODEINE
Product Number
4
Dosage Form
-
Strength
325MG;60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85056
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL W/ CODEINE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85057
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL W/ CODEINE NO. 3
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87422
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL W/ CODEINE NO. 4
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87421
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL WITH NAPROXEN
Product Number
1
Dosage Form
-
Strength
325MG;110MG
Approval Date
Jul 24, 2026
Active Ingredient
ACETAMINOPHEN; NAPROXEN SODIUM
Identifiers
Application No.: 219962
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;110MG
Approval Date
Jul 24, 2026
Regulatory Status
OTC
Drug Name
TYLOX
Product Number
1
Dosage Form
-
Strength
500MG;4.5MG;0.38MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE; OXYCODONE TEREPHTHALATE
Identifiers
Application No.: 85375
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;4.5MG;0.38MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLOX-325
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Nov 08, 1984
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 88246
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Nov 08, 1984
Regulatory Status
Discontinued
Drug Name
ZYFREL
Product Number
1
Dosage Form
-
Strength
325MG/15ML;7.5MG/15ML
Approval Date
Apr 14, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90468
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/15ML;7.5MG/15ML
Approval Date
Apr 14, 2016
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Apr 18, 2023
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 205746
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Apr 18, 2023
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Apr 15, 2013
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 202800
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Apr 15, 2013
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;30MG
Approval Date
Apr 15, 2013
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 202800
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Apr 15, 2013
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
3
Dosage Form
-
Strength
300MG;60MG
Approval Date
Apr 15, 2013
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 202800
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Apr 15, 2013
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Sep 26, 2018
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 204733
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Sep 26, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Apr 11, 2012
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 201013
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Apr 11, 2012
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Apr 11, 2012
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 201013
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Apr 11, 2012
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Apr 11, 2012
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 201013
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Apr 11, 2012
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Sep 13, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207709
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Sep 13, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Sep 13, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207709
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Sep 13, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Sep 13, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207709
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Sep 13, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Jul 15, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201972
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Jul 15, 2013
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jul 15, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201972
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jul 15, 2013
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jul 15, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201972
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jul 15, 2013
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jul 15, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201972
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jul 15, 2013
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;2.5MG
Approval Date
Jul 26, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40307
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;2.5MG
Approval Date
Jul 26, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Jul 26, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40307
Product No.: 2
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Jul 26, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Jul 26, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40307
Product No.: 3
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Jul 26, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
650MG;10MG
Approval Date
Jul 26, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40307
Product No.: 4
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Jul 26, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jul 26, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40308
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jul 26, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Jul 26, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40308
Product No.: 2
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Jul 26, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;10MG
Approval Date
Jul 26, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40309
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
Jul 26, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Dec 21, 1984
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 88577
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Dec 21, 1984
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Oct 02, 2000
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40304
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Oct 02, 2000
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 87406
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90265
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90265
Product No.: 2
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
500MG;10MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90265
Product No.: 3
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90380
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG;10MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90380
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
660MG;10MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90380
Product No.: 3
Product
Dosage Form: -
Strength: 660MG;10MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90380
Product No.: 4
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
WYGESIC
Product Number
1
Dosage Form
-
Strength
650MG;65MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE
Identifiers
Application No.: 84999
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;65MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Sep 10, 2019
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 212418
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Sep 10, 2019
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;30MG
Approval Date
Sep 10, 2019
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 212418
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Sep 10, 2019
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
3
Dosage Form
-
Strength
300MG;60MG
Approval Date
Sep 10, 2019
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 212418
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Sep 10, 2019
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Nov 16, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209924
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Nov 16, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Nov 16, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209924
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Nov 16, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Nov 16, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209924
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Nov 16, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Nov 16, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209924
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Nov 16, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jul 02, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 209385
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jul 02, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jul 02, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 209385
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jul 02, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jul 02, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 209385
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jul 02, 2018
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
500MG;50MG;40MG
Approval Date
Aug 25, 2003
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40513
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;50MG;40MG
Approval Date
Aug 25, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;10MG
Approval Date
Feb 22, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40143
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Feb 22, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Feb 22, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40144
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Feb 22, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
500MG;2.5MG
Approval Date
Apr 25, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40144
Product No.: 2
Product
Dosage Form: -
Strength: 500MG;2.5MG
Approval Date
Apr 25, 1997
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Apr 14, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40155
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Apr 14, 1997
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Apr 12, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40157
Product No.: 1
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Apr 12, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Sep 30, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40280
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Sep 30, 1998
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Sep 30, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40280
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Sep 30, 1998
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
650MG;10MG
Approval Date
Sep 30, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40280
Product No.: 3
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Sep 30, 1998
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Sep 30, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40281
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Sep 30, 1998
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Sep 30, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40281
Product No.: 2
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Sep 30, 1998
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;10MG
Approval Date
May 31, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40356
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
May 31, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
660MG;10MG
Approval Date
May 31, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40358
Product No.: 1
Product
Dosage Form: -
Strength: 660MG;10MG
Approval Date
May 31, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/15ML;7.5MG/15ML
Approval Date
Oct 30, 2003
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40520
Product No.: 1
Product
Dosage Form: -
Strength: 500MG/15ML;7.5MG/15ML
Approval Date
Oct 30, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Sep 07, 1988
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89831
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Sep 07, 1988
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Dec 02, 1988
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89971
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Dec 02, 1988
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jul 30, 1996
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40106
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jul 30, 1996
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Dec 30, 1999
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40303
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Dec 30, 1999
Regulatory Status
Discontinued
Drug Name
PERCOCET
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Jul 26, 1999
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40341
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Jul 26, 1999
Regulatory Status
Discontinued
Drug Name
PERCOCET
Product Number
2
Dosage Form
-
Strength
650MG;10MG
Approval Date
Jul 26, 1999
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40341
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Jul 26, 1999
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;65MG
Approval Date
Jul 30, 2003
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE
Identifiers
Application No.: 40507
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;65MG
Approval Date
Jul 30, 2003
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Feb 12, 1997
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 74843
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Feb 12, 1997
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;50MG
Approval Date
Feb 15, 2001
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 74843
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Feb 15, 2001
Regulatory Status
Discontinued
Drug Name
ZYDONE
Product Number
1
Dosage Form
-
Strength
400MG;5MG
Approval Date
Nov 27, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40288
Product No.: 1
Product
Dosage Form: -
Strength: 400MG;5MG
Approval Date
Nov 27, 1998
Regulatory Status
Discontinued
Drug Name
ZYDONE
Product Number
2
Dosage Form
-
Strength
400MG;7.5MG
Approval Date
Nov 27, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40288
Product No.: 2
Product
Dosage Form: -
Strength: 400MG;7.5MG
Approval Date
Nov 27, 1998
Regulatory Status
Discontinued
Drug Name
ZYDONE
Product Number
3
Dosage Form
-
Strength
400MG;10MG
Approval Date
Nov 27, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40288
Product No.: 3
Product
Dosage Form: -
Strength: 400MG;10MG
Approval Date
Nov 27, 1998
Regulatory Status
Discontinued
Drug Name
ALLAY
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jan 13, 1989
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89907
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jan 13, 1989
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Apr 21, 1988
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89696
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Apr 21, 1988
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Aug 02, 1985
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70146
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Aug 02, 1985
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
500MG;50MG;40MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40883
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;50MG;40MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Feb 11, 2008
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 77821
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Feb 11, 2008
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85794
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85795
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Apr 13, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87653
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Apr 13, 1982
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Sep 25, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40236
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Sep 25, 1997
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Sep 25, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40236
Product No.: 2
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Sep 25, 1997
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;10MG
Approval Date
Nov 26, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40240
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Nov 26, 1997
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Nov 26, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40240
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Nov 26, 1997
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jan 22, 1998
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40219
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jan 22, 1998
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Jun 12, 1985
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70115
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Jun 12, 1985
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Jun 12, 1985
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70116
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Jun 12, 1985
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Mar 21, 1986
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70615
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Mar 21, 1986
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Mar 21, 1986
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70771
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Mar 21, 1986
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Mar 21, 1986
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70775
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Mar 21, 1986
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jul 17, 2020
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 211543
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jul 17, 2020
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/15ML;7.5MG/15ML
Approval Date
Jan 23, 2002
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40366
Product No.: 1
Product
Dosage Form: -
Strength: 500MG/15ML;7.5MG/15ML
Approval Date
Jan 23, 2002
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Dec 28, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 210079
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Dec 28, 2017
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Dec 28, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 210079
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Dec 28, 2017
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Dec 28, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 210079
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Dec 28, 2017
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Dec 28, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 210079
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Dec 28, 2017
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Nov 14, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206142
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Nov 14, 2016
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Nov 14, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206142
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Nov 14, 2016
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Nov 14, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206142
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Nov 14, 2016
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Dec 01, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206245
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Dec 01, 2016
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Dec 01, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206245
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Dec 01, 2016
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Dec 01, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206245
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Dec 01, 2016
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Feb 24, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 204407
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Feb 24, 2017
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Feb 24, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 204407
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Feb 24, 2017
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Feb 24, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 204407
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Feb 24, 2017
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Feb 24, 2017
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 204407
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Feb 24, 2017
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85218
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85992
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87306
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE
Product Number
1
Dosage Form
-
Strength
712.8MG;60MG;32MG
Approval Date
Sep 22, 2006
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Identifiers
Application No.: 40637
Product No.: 1
Product
Dosage Form: -
Strength: 712.8MG;60MG;32MG
Approval Date
Sep 22, 2006
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Oct 30, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 210211
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Oct 30, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Oct 30, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 210211
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Oct 30, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Oct 30, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 210211
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Oct 30, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/15ML;7.5MG/15ML
Approval Date
Mar 08, 2019
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 211023
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/15ML;7.5MG/15ML
Approval Date
Mar 08, 2019
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Mar 21, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207510
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Mar 21, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Mar 21, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207510
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Mar 21, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Mar 21, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207510
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Mar 21, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
500MG;10MG
Approval Date
Feb 14, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40148
Product No.: 2
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
Feb 14, 1997
Regulatory Status
Discontinued
Drug Name
NORCO
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jun 25, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40099
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jun 25, 1997
Regulatory Status
Discontinued
Drug Name
NORCO
Product Number
1
Dosage Form
-
Strength
325MG;10MG
Approval Date
Feb 14, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40148
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Feb 14, 1997
Regulatory Status
Discontinued
Drug Name
NORCO
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Sep 12, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40148
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Sep 12, 2000
Regulatory Status
Discontinued
Drug Name
NORCO
Product Number
4
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Jul 07, 2014
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40148
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Jul 07, 2014
Regulatory Status
Discontinued
Drug Name
NORCO
Product Number
5
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jul 07, 2014
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40148
Product No.: 5
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jul 07, 2014
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Aug 01, 2023
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 216999
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Aug 01, 2023
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Sep 20, 1996
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40098
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Sep 20, 1996
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Nov 18, 1997
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40223
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Nov 18, 1997
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;30MG
Approval Date
Nov 18, 1997
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40223
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Nov 18, 1997
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
3
Dosage Form
-
Strength
300MG;60MG
Approval Date
Nov 18, 1997
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40223
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Nov 18, 1997
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Feb 06, 1984
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88353
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Feb 06, 1984
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Feb 06, 1984
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88354
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Feb 06, 1984
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Feb 06, 1984
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88355
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Feb 06, 1984
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jun 30, 1998
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40272
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jun 30, 1998
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Mar 16, 1999
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40289
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Mar 16, 1999
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND PENTAZOCINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
650MG;EQ 25MG BASE
Approval Date
Aug 02, 2002
Active Ingredient
ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE
Identifiers
Application No.: 76202
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;EQ 25MG BASE
Approval Date
Aug 02, 2002
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/15ML;7.5MG/15ML
Approval Date
Mar 13, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40182
Product No.: 1
Product
Dosage Form: -
Strength: 500MG/15ML;7.5MG/15ML
Approval Date
Mar 13, 1998
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/15ML;10MG/15ML
Approval Date
Apr 18, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40834
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/15ML;10MG/15ML
Approval Date
Apr 18, 2008
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/15ML;7.5MG/15ML
Approval Date
May 10, 2013
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40838
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/15ML;7.5MG/15ML
Approval Date
May 10, 2013
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Dec 10, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87762
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Dec 10, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 86681
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 86683
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jul 17, 1986
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89080
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jul 17, 1986
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Feb 10, 1988
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89673
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Feb 10, 1988
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;15MG
Approval Date
Feb 10, 1988
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89673
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Feb 10, 1988
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
3
Dosage Form
-
Strength
300MG;30MG
Approval Date
Feb 10, 1988
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89673
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Feb 10, 1988
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Apr 12, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202991
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Apr 12, 2016
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Apr 12, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202991
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Apr 12, 2016
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Apr 12, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202991
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Apr 12, 2016
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Mar 30, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207808
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Mar 30, 2018
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Mar 30, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207808
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Mar 30, 2018
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Mar 30, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207808
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Mar 30, 2018
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Aug 28, 2014
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201278
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Aug 28, 2014
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Aug 28, 2014
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201278
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Aug 28, 2014
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Aug 28, 2014
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201278
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Aug 28, 2014
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 84656
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 84659
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 84667
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
500MG;15MG
Approval Date
Apr 25, 1989
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89511
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;15MG
Approval Date
Apr 25, 1989
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
500MG;30MG
Approval Date
Apr 25, 1989
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89512
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;30MG
Approval Date
Apr 25, 1989
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
500MG;60MG
Approval Date
Apr 25, 1989
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89513
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;60MG
Approval Date
Apr 25, 1989
Regulatory Status
Discontinued
Drug Name
ROXICET 5/500
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jan 12, 1989
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 89775
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jan 12, 1989
Regulatory Status
Discontinued
Drug Name
ROXILOX
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jul 03, 1995
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40061
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jul 03, 1995
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jun 22, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87919
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jun 22, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jun 22, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87920
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jun 22, 1982
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
May 29, 1987
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89290
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
May 29, 1987
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
May 29, 1987
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89291
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
May 29, 1987
Regulatory Status
Discontinued
Drug Name
DARVOCET
Product Number
1
Dosage Form
-
Strength
325MG;32.5MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE
Identifiers
Application No.: 16844
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;32.5MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
VICODIN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jan 07, 1983
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 88058
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jan 07, 1983
Regulatory Status
Discontinued
Drug Name
VICODIN ES
Product Number
1
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Dec 09, 1988
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89736
Product No.: 1
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Dec 09, 1988
Regulatory Status
Discontinued
Drug Name
VICODIN HP
Product Number
1
Dosage Form
-
Strength
660MG;10MG
Approval Date
Sep 23, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40117
Product No.: 1
Product
Dosage Form: -
Strength: 660MG;10MG
Approval Date
Sep 23, 1996
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Jan 22, 2003
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40443
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Jan 22, 2003
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 22, 2003
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40443
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 22, 2003
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
3
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 22, 2003
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40443
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 22, 2003
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85861
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
May 26, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87275
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
May 26, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
May 26, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87276
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
May 26, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
May 26, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87277
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
May 26, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND PENTAZOCINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
650MG;EQ 25MG BASE
Approval Date
Mar 24, 2000
Active Ingredient
ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE
Identifiers
Application No.: 74699
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;EQ 25MG BASE
Approval Date
Mar 24, 2000
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
325MG; 7.5MG
Approval Date
-
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 207113
Product No.: 1
Product
Dosage Form: -
Strength: 325MG; 7.5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Oct 19, 1984
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 87550
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Oct 19, 1984
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
500MG;50MG;40MG
Approval Date
Jul 30, 1998
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40267
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;50MG;40MG
Approval Date
Jul 30, 1998
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Nov 09, 1984
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 88616
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Nov 09, 1984
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Feb 16, 1988
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 89536
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Feb 16, 1988
Regulatory Status
Discontinued
Drug Name
CAPITAL AND CODEINE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85883
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
CODRIX
Product Number
1
Dosage Form
-
Strength
500MG;30MG
Approval Date
Mar 27, 2003
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40441
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;30MG
Approval Date
Mar 27, 2003
Regulatory Status
Discontinued
Drug Name
CODRIX
Product Number
1
Dosage Form
-
Strength
500MG;15MG
Approval Date
Feb 26, 2003
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40447
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;15MG
Approval Date
Feb 26, 2003
Regulatory Status
Discontinued
Drug Name
CODRIX
Product Number
1
Dosage Form
-
Strength
500MG;60MG
Approval Date
Mar 28, 2003
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40488
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;60MG
Approval Date
Mar 28, 2003
Regulatory Status
Discontinued
Drug Name
FIORICET W/ CODEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG;30MG
Approval Date
Jul 30, 1992
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 20232
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG;30MG
Approval Date
Jul 30, 1992
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Sep 29, 1995
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40094
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Sep 29, 1995
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG;10MG
Approval Date
Sep 29, 1995
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40094
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Sep 29, 1995
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
660MG;10MG
Approval Date
Aug 08, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40094
Product No.: 3
Product
Dosage Form: -
Strength: 660MG;10MG
Approval Date
Aug 08, 2000
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
750MG;10MG
Approval Date
Mar 22, 1999
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40094
Product No.: 4
Product
Dosage Form: -
Strength: 750MG;10MG
Approval Date
Mar 22, 1999
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Mar 04, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40122
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Mar 04, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Mar 04, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40122
Product No.: 2
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Mar 04, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Mar 04, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40123
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Mar 04, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG;10MG
Approval Date
Mar 04, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40123
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Mar 04, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
500MG;2.5MG
Approval Date
Mar 04, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40123
Product No.: 3
Product
Dosage Form: -
Strength: 500MG;2.5MG
Approval Date
Mar 04, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Mar 04, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40123
Product No.: 4
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Mar 04, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
May 28, 2003
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40493
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
May 28, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
May 28, 2003
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40494
Product No.: 1
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
May 28, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
660MG;10MG
Approval Date
May 28, 2003
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40495
Product No.: 1
Product
Dosage Form: -
Strength: 660MG;10MG
Approval Date
May 28, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;2.5MG
Approval Date
Aug 30, 1991
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 81079
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;2.5MG
Approval Date
Aug 30, 1991
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Aug 30, 1991
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 81080
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Aug 30, 1991
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Aug 30, 1991
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 81083
Product No.: 1
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Aug 30, 1991
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Dec 01, 1988
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89883
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Dec 01, 1988
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Jun 02, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206470
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Jun 02, 2016
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Jun 02, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206470
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Jun 02, 2016
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Jun 02, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206470
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Jun 02, 2016
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Oct 30, 1997
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40171
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Oct 30, 1997
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Dec 30, 1998
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40199
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Dec 30, 1998
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Mar 15, 1999
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40203
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Mar 15, 1999
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Oct 30, 1997
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40234
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Oct 30, 1997
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Dec 29, 2000
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40371
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Dec 29, 2000
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG;10MG
Approval Date
Dec 29, 2000
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40371
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Dec 29, 2000
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Sep 05, 2003
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40535
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Sep 05, 2003
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;10MG
Approval Date
Sep 05, 2003
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40535
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Sep 05, 2003
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Apr 03, 2012
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40800
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Apr 03, 2012
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;10MG
Approval Date
Apr 03, 2012
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40800
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Apr 03, 2012
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Apr 12, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201447
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Apr 12, 2013
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Apr 12, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201447
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Apr 12, 2013
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Apr 12, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201447
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Apr 12, 2013
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Apr 12, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 201447
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Apr 12, 2013
Regulatory Status
RX
Drug Name
PROPOXYPHENE HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;65MG
Approval Date
Dec 16, 1996
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE
Identifiers
Application No.: 40139
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;65MG
Approval Date
Dec 16, 1996
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Dec 18, 1986
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70398
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Dec 18, 1986
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Dec 18, 1986
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70399
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Dec 18, 1986
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Jan 02, 1987
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70910
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Jan 02, 1987
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Nov 16, 2004
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 76609
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Nov 16, 2004
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;100MG
Approval Date
Jun 28, 2005
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 77196
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;100MG
Approval Date
Jun 28, 2005
Regulatory Status
Discontinued
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
Mar 30, 2012
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 202076
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
Mar 30, 2012
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;10MG
Approval Date
Nov 29, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 207137
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Nov 29, 2016
Regulatory Status
Discontinued
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
Dec 09, 2009
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 90485
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
Dec 09, 2009
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Mar 06, 1985
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88629
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Mar 06, 1985
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;15MG
Approval Date
Mar 06, 1985
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88629
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Mar 06, 1985
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
3
Dosage Form
-
Strength
300MG;30MG
Approval Date
Mar 06, 1985
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88629
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Mar 06, 1985
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Dec 29, 1983
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88324
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Dec 29, 1983
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Jun 04, 1984
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88537
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Jun 04, 1984
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jun 01, 1984
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 88599
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jun 01, 1984
Regulatory Status
Discontinued
Drug Name
PROPACET 100
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Jun 12, 1985
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70107
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Jun 12, 1985
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Jan 03, 1986
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70732
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Jan 03, 1986
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Dec 19, 1994
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 74119
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Dec 19, 1994
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Nov 09, 2016
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 207229
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Nov 09, 2016
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Mar 26, 2024
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 218359
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Mar 26, 2024
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN, ASPIRIN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
250MG;250MG;65MG
Approval Date
Feb 02, 2022
Active Ingredient
ACETAMINOPHEN; ASPIRIN; CAFFEINE
Identifiers
Application No.: 211695
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;250MG;65MG
Approval Date
Feb 02, 2022
Regulatory Status
OTC
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
Mar 22, 2017
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 207152
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
Mar 22, 2017
Regulatory Status
RX
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Sep 17, 2021
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 214331
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Sep 17, 2021
Regulatory Status
RX
Drug Name
ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG/65ML (10MG/ML)
Approval Date
May 21, 2025
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 214331
Product No.: 2
Product
Dosage Form: -
Strength: 650MG/65ML (10MG/ML)
Approval Date
May 21, 2025
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Mar 30, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 203863
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Mar 30, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Mar 30, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 203863
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Mar 30, 2018
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Mar 30, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 203863
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Mar 30, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Jul 02, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 203864
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Jul 02, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jul 02, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 203864
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jul 02, 2018
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jul 02, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 203864
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jul 02, 2018
Regulatory Status
RX
Drug Name
BANCAP
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Jan 16, 1986
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 88889
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Jan 16, 1986
Regulatory Status
Discontinued
Drug Name
BANCAP HC
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Mar 17, 1983
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 87961
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Mar 17, 1983
Regulatory Status
Discontinued
Drug Name
DURADYNE DHC
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Mar 17, 1983
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 87809
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Mar 17, 1983
Regulatory Status
Discontinued
Drug Name
ESGIC
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Dec 23, 1988
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 89660
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Dec 23, 1988
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/50ML (10MG/ML)
Approval Date
Apr 02, 2025
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 219215
Product No.: 1
Product
Dosage Form: -
Strength: 500MG/50ML (10MG/ML)
Approval Date
Apr 02, 2025
Regulatory Status
RX
Drug Name
ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Apr 02, 2025
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 219215
Product No.: 2
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Apr 02, 2025
Regulatory Status
RX
Drug Name
EMPRACET W/ CODEINE PHOSPHATE #3
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 83951
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
EMPRACET W/ CODEINE PHOSPHATE #4
Product Number
2
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 83951
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Apr 16, 2019
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 211544
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Apr 16, 2019
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN, ASPIRIN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
250MG;250MG;65MG
Approval Date
Feb 23, 2021
Active Ingredient
ACETAMINOPHEN; ASPIRIN; CAFFEINE
Identifiers
Application No.: 214039
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;250MG;65MG
Approval Date
Feb 23, 2021
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Jun 13, 2016
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 202605
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Jun 13, 2016
Regulatory Status
RX
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Jun 03, 2022
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 206968
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Jun 03, 2022
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
500MG;50MG;40MG
Approval Date
Oct 28, 1998
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40261
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;50MG;40MG
Approval Date
Oct 28, 1998
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
500MG;50MG;40MG
Approval Date
Aug 18, 1999
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40336
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;50MG;40MG
Approval Date
Aug 18, 1999
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jun 12, 1995
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 89718
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jun 12, 1995
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Mar 25, 2022
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 215135
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Mar 25, 2022
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
2
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Mar 25, 2022
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 215135
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Mar 25, 2022
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN, CAFFEINE AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG;30MG
Approval Date
Mar 23, 2001
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 75618
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG;30MG
Approval Date
Mar 23, 2001
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN, CAFFEINE AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG;30MG
Approval Date
Jan 26, 2022
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 215138
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG;30MG
Approval Date
Jan 26, 2022
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN, CAFFEINE AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;50MG;40MG;30MG
Approval Date
Jan 26, 2022
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 215138
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;50MG;40MG;30MG
Approval Date
Jan 26, 2022
Regulatory Status
RX
Drug Name
COMBOGESIC IV
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML);EQ 300MG BASE/100ML (EQ 3MG BASE/ML)
Approval Date
Oct 17, 2023
Active Ingredient
ACETAMINOPHEN; IBUPROFEN SODIUM
Identifiers
Application No.: 215320
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML);EQ 300MG BASE/100ML (EQ 3MG BASE/ML)
Approval Date
Oct 17, 2023
Regulatory Status
RX
Drug Name
ROXICET
Product Number
1
Dosage Form
-
Strength
325MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 87003
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ROXICET
Product Number
1
Dosage Form
-
Strength
325MG/5ML;5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Dec 03, 1986
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 89351
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/5ML;5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Dec 03, 1986
Regulatory Status
Discontinued
Drug Name
TYLENOL W/ CODEINE NO. 1
Product Number
1
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85055
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL W/ CODEINE NO. 2
Product Number
2
Dosage Form
-
Strength
300MG;15MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85055
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL W/ CODEINE NO. 3
Product Number
3
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85055
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLENOL W/ CODEINE NO. 4
Product Number
4
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85055
Product No.: 4
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
TYLOX
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Dec 12, 1984
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 88790
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Dec 12, 1984
Regulatory Status
Discontinued
Drug Name
ULTRACET
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Aug 15, 2001
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 21123
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Aug 15, 2001
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
120MG
Approval Date
Apr 06, 1987
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 70607
Product No.: 1
Product
Dosage Form: -
Strength: 120MG
Approval Date
Apr 06, 1987
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Dec 01, 1986
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 70608
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Dec 01, 1986
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Feb 25, 2000
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 75077
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Feb 25, 2000
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN, ASPIRIN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
250MG;250MG;65MG
Approval Date
Nov 26, 2001
Active Ingredient
ACETAMINOPHEN; ASPIRIN; CAFFEINE
Identifiers
Application No.: 75794
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;250MG;65MG
Approval Date
Nov 26, 2001
Regulatory Status
OTC
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
May 02, 2017
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 206885
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
May 02, 2017
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
May 31, 2001
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40419
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
May 31, 2001
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;30MG
Approval Date
May 31, 2001
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40419
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
May 31, 2001
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
3
Dosage Form
-
Strength
300MG;60MG
Approval Date
May 31, 2001
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40419
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
May 31, 2001
Regulatory Status
RX
Drug Name
ANEXSIA
Product Number
1
Dosage Form
-
Strength
750MG;10MG
Approval Date
Oct 31, 2002
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40468
Product No.: 1
Product
Dosage Form: -
Strength: 750MG;10MG
Approval Date
Oct 31, 2002
Regulatory Status
Discontinued
Drug Name
ANEXSIA
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Apr 23, 1987
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89160
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Apr 23, 1987
Regulatory Status
Discontinued
Drug Name
ANEXSIA 5/325
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Oct 20, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40409
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Oct 20, 2000
Regulatory Status
RX
Drug Name
ANEXSIA 7.5/325
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Sep 08, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40405
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Sep 08, 2000
Regulatory Status
RX
Drug Name
ANEXSIA 7.5/650
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Sep 30, 1987
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89725
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Sep 30, 1987
Regulatory Status
Discontinued
Drug Name
BUCET
Product Number
1
Dosage Form
-
Strength
650MG;50MG
Approval Date
Jun 28, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 88991
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;50MG
Approval Date
Jun 28, 1985
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jan 24, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 87804
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jan 24, 1985
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jul 18, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 88743
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jul 18, 1985
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Mar 27, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 88758
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Mar 27, 1985
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Mar 27, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 88765
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Mar 27, 1985
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Apr 19, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 89067
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Apr 19, 1985
Regulatory Status
Discontinued
Drug Name
FEMCET
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jun 19, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 89102
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jun 19, 1985
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Jun 01, 1995
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40084
Product No.: 1
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Jun 01, 1995
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jun 01, 1995
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40084
Product No.: 2
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jun 01, 1995
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
660MG;10MG
Approval Date
Jul 29, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40084
Product No.: 3
Product
Dosage Form: -
Strength: 660MG;10MG
Approval Date
Jul 29, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
650MG;10MG
Approval Date
Oct 16, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40084
Product No.: 4
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Oct 16, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Feb 27, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40201
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Feb 27, 1998
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
500MG;10MG
Approval Date
Feb 27, 1998
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40201
Product No.: 2
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
Feb 27, 1998
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jul 26, 2000
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40400
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jul 26, 2000
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/15ML;7.5MG/15ML
Approval Date
Jun 27, 2001
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40418
Product No.: 1
Product
Dosage Form: -
Strength: 500MG/15ML;7.5MG/15ML
Approval Date
Jun 27, 2001
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/15ML;10MG/15ML
Approval Date
Aug 29, 2003
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40508
Product No.: 1
Product
Dosage Form: -
Strength: 500MG/15ML;10MG/15ML
Approval Date
Aug 29, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jul 19, 1985
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 88956
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jul 19, 1985
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Aug 09, 1985
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89006
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Aug 09, 1985
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Mar 31, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206718
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Mar 31, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Mar 31, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206718
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Mar 31, 2017
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Mar 31, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206718
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Mar 31, 2017
Regulatory Status
RX
Drug Name
LORCET-HD
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jul 08, 1982
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 87336
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jul 08, 1982
Regulatory Status
Discontinued
Drug Name
OXYCET
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Dec 07, 1983
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 87463
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Dec 07, 1983
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Aug 04, 1998
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40257
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Aug 04, 1998
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jun 30, 2004
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40545
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jun 30, 2004
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jun 30, 2004
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40545
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jun 30, 2004
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Jun 30, 2004
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40550
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Jun 30, 2004
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG;10MG
Approval Date
Jun 30, 2004
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40550
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Jun 30, 2004
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/5ML;5MG/5ML
Approval Date
Sep 29, 2006
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40680
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/5ML;5MG/5ML
Approval Date
Sep 29, 2006
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Feb 02, 2001
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 75738
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Feb 02, 2001
Regulatory Status
Discontinued
Drug Name
TENCON
Product Number
1
Dosage Form
-
Strength
650MG;50MG
Approval Date
May 15, 1990
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 89405
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;50MG
Approval Date
May 15, 1990
Regulatory Status
Discontinued
Drug Name
TRIAD
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jun 19, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 89023
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jun 19, 1985
Regulatory Status
Discontinued
Drug Name
XARTEMIS XR
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Mar 11, 2014
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 204031
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Mar 11, 2014
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Aug 25, 2021
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 215486
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Aug 25, 2021
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Jul 10, 2023
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 216994
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Jul 10, 2023
Regulatory Status
OTC
Drug Name
DRIXORAL PLUS
Product Number
1
Dosage Form
-
Strength
500MG;3MG;60MG
Approval Date
May 22, 1987
Active Ingredient
ACETAMINOPHEN; DEXBROMPHENIRAMINE MALEATE; PSEUDOEPHEDRINE SULFATE
Identifiers
Application No.: 19453
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;3MG;60MG
Approval Date
May 22, 1987
Regulatory Status
Discontinued
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
Dec 14, 2012
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 201952
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
Dec 14, 2012
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
650MG;30MG
Approval Date
Mar 03, 1986
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89231
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;30MG
Approval Date
Mar 03, 1986
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Feb 25, 1986
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89238
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Feb 25, 1986
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Feb 25, 1986
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89244
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Feb 25, 1986
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
650MG;60MG
Approval Date
Sep 09, 1991
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 89363
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;60MG
Approval Date
Sep 09, 1991
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN, ASPIRIN, AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
150MG;180MG;15MG
Approval Date
Oct 26, 1990
Active Ingredient
ACETAMINOPHEN; ASPIRIN; CODEINE PHOSPHATE
Identifiers
Application No.: 81095
Product No.: 1
Product
Dosage Form: -
Strength: 150MG;180MG;15MG
Approval Date
Oct 26, 1990
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN, ASPIRIN, AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
150MG;180MG;30MG
Approval Date
Oct 26, 1990
Active Ingredient
ACETAMINOPHEN; ASPIRIN; CODEINE PHOSPHATE
Identifiers
Application No.: 81096
Product No.: 1
Product
Dosage Form: -
Strength: 150MG;180MG;30MG
Approval Date
Oct 26, 1990
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN, ASPIRIN, AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
150MG;180MG;60MG
Approval Date
Oct 26, 1990
Active Ingredient
ACETAMINOPHEN; ASPIRIN; CODEINE PHOSPHATE
Identifiers
Application No.: 81097
Product No.: 1
Product
Dosage Form: -
Strength: 150MG;180MG;60MG
Approval Date
Oct 26, 1990
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE
Product Number
1
Dosage Form
-
Strength
356.4MG;30MG;16MG
Approval Date
Aug 26, 1997
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Identifiers
Application No.: 40109
Product No.: 1
Product
Dosage Form: -
Strength: 356.4MG;30MG;16MG
Approval Date
Aug 26, 1997
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE
Product Number
1
Dosage Form
-
Strength
712.8MG;60MG;32MG
Approval Date
Apr 28, 1999
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Identifiers
Application No.: 40316
Product No.: 1
Product
Dosage Form: -
Strength: 712.8MG;60MG;32MG
Approval Date
Apr 28, 1999
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
750MG;50MG;40MG
Approval Date
Dec 23, 2003
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40496
Product No.: 1
Product
Dosage Form: -
Strength: 750MG;50MG;40MG
Approval Date
Dec 23, 2003
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jan 21, 1987
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 89175
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jan 21, 1987
Regulatory Status
RX
Drug Name
BUTAPAP
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Oct 26, 1992
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 89987
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Oct 26, 1992
Regulatory Status
RX
Drug Name
BUTAPAP
Product Number
1
Dosage Form
-
Strength
650MG;50MG
Approval Date
Oct 26, 1992
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 89988
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;50MG
Approval Date
Oct 26, 1992
Regulatory Status
Discontinued
Drug Name
ESGIC-PLUS
Product Number
1
Dosage Form
-
Strength
500MG;50MG;40MG
Approval Date
Mar 28, 1996
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40085
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;50MG;40MG
Approval Date
Mar 28, 1996
Regulatory Status
Discontinued
Drug Name
ESGIC-PLUS
Product Number
1
Dosage Form
-
Strength
500MG;50MG;40MG
Approval Date
May 23, 1988
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 89451
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;50MG;40MG
Approval Date
May 23, 1988
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Jun 09, 2010
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40846
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Jun 09, 2010
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;5MG
Approval Date
Jun 09, 2010
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40849
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;5MG
Approval Date
Jun 09, 2010
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG/15ML;10MG/15ML
Approval Date
Feb 25, 2010
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40881
Product No.: 1
Product
Dosage Form: -
Strength: 300MG/15ML;10MG/15ML
Approval Date
Feb 25, 2010
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/15ML;7.5MG/15ML
Approval Date
Aug 28, 1992
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 81051
Product No.: 1
Product
Dosage Form: -
Strength: 500MG/15ML;7.5MG/15ML
Approval Date
Aug 28, 1992
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Nov 30, 1989
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 81067
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Nov 30, 1989
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Nov 30, 1989
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 81068
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Nov 30, 1989
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Nov 30, 1989
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 81069
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Nov 30, 1989
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Nov 30, 1989
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 81070
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Nov 30, 1989
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;10MG
Approval Date
May 29, 1992
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 81223
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
May 29, 1992
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/15ML;5MG/15ML
Approval Date
Oct 27, 1992
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 81226
Product No.: 1
Product
Dosage Form: -
Strength: 500MG/15ML;5MG/15ML
Approval Date
Oct 27, 1992
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Feb 21, 1986
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89008
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Feb 21, 1986
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jul 16, 1986
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89271
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jul 16, 1986
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/15ML;5MG/15ML
Approval Date
Apr 29, 1992
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89557
Product No.: 1
Product
Dosage Form: -
Strength: 500MG/15ML;5MG/15ML
Approval Date
Apr 29, 1992
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Jun 29, 1988
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89689
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Jun 29, 1988
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jan 28, 1992
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89697
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jan 28, 1992
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;2.5MG
Approval Date
Aug 25, 1989
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89698
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;2.5MG
Approval Date
Aug 25, 1989
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
Aug 25, 1989
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 89699
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
Aug 25, 1989
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;2.5MG
Approval Date
Dec 30, 2005
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40608
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;2.5MG
Approval Date
Dec 30, 2005
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;5MG
Approval Date
Dec 30, 2005
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40608
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Dec 30, 2005
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Dec 30, 2005
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40608
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Dec 30, 2005
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
300MG;10MG
Approval Date
Dec 30, 2005
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40608
Product No.: 4
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Dec 30, 2005
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;10MG
Approval Date
Apr 19, 2006
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40676
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
Apr 19, 2006
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
400MG;2.5MG
Approval Date
May 16, 2006
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40679
Product No.: 1
Product
Dosage Form: -
Strength: 400MG;2.5MG
Approval Date
May 16, 2006
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
400MG;5MG
Approval Date
Apr 27, 2006
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40687
Product No.: 1
Product
Dosage Form: -
Strength: 400MG;5MG
Approval Date
Apr 27, 2006
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
400MG;10MG
Approval Date
Apr 27, 2006
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40692
Product No.: 1
Product
Dosage Form: -
Strength: 400MG;10MG
Approval Date
Apr 27, 2006
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
400MG;7.5MG
Approval Date
Apr 27, 2006
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 40698
Product No.: 1
Product
Dosage Form: -
Strength: 400MG;7.5MG
Approval Date
Apr 27, 2006
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG/5ML;10MG/5ML
Approval Date
Nov 27, 2018
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 202142
Product No.: 1
Product
Dosage Form: -
Strength: 300MG/5ML;10MG/5ML
Approval Date
Nov 27, 2018
Regulatory Status
RX
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Aug 07, 2020
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 213255
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Aug 07, 2020
Regulatory Status
RX
Drug Name
PROPOXYPHENE HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;32MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE
Identifiers
Application No.: 83689
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;32MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;65MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE
Identifiers
Application No.: 83978
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;65MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Jun 12, 1985
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70145
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Jun 12, 1985
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Feb 16, 1988
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 72195
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Feb 16, 1988
Regulatory Status
Discontinued
Drug Name
TAVIST ALLERGY/SINUS/HEADACHE
Product Number
1
Dosage Form
-
Strength
500MG;EQ 0.25MG BASE;30MG
Approval Date
Mar 01, 2001
Active Ingredient
ACETAMINOPHEN; CLEMASTINE FUMARATE; PSEUDOEPHEDRINE HYDROCHLORIDE
Identifiers
Application No.: 21082
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;EQ 0.25MG BASE;30MG
Approval Date
Mar 01, 2001
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Mar 19, 2002
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 76200
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Mar 19, 2002
Regulatory Status
OTC
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Aug 16, 2007
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40822
Product No.: 1
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Aug 16, 2007
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;10MG
Approval Date
Aug 16, 2007
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40824
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
Aug 16, 2007
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Aug 16, 2007
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40825
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Aug 16, 2007
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Mar 22, 2016
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 204052
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Mar 22, 2016
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85291
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85917
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85964
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87423
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;15MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87433
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;15MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jan 27, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40149
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jan 27, 1997
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Jan 27, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40149
Product No.: 2
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Jan 27, 1997
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;65MG
Approval Date
Jul 18, 1989
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE
Identifiers
Application No.: 89959
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;65MG
Approval Date
Jul 18, 1989
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Jan 23, 1986
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 70443
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Jan 23, 1986
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
120MG
Approval Date
Feb 27, 1995
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 73106
Product No.: 1
Product
Dosage Form: -
Strength: 120MG
Approval Date
Feb 27, 1995
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG
Approval Date
Feb 27, 1995
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 73107
Product No.: 1
Product
Dosage Form: -
Strength: 325MG
Approval Date
Feb 27, 1995
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Feb 27, 1995
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 73108
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Feb 27, 1995
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Dec 14, 2011
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 78569
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Dec 14, 2011
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG
Approval Date
Nov 18, 2009
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 90205
Product No.: 1
Product
Dosage Form: -
Strength: 650MG
Approval Date
Nov 18, 2009
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Aug 01, 2002
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40452
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Aug 01, 2002
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Aug 01, 2002
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 40459
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Aug 01, 2002
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85868
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87083
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;60MG
Approval Date
Jan 01, 1982
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jul 23, 2001
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40390
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jul 23, 2001
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
500MG;50MG;40MG
Approval Date
Jul 23, 2001
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40394
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;50MG;40MG
Approval Date
Jul 23, 2001
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN, CAFFEINE AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG;30MG
Approval Date
Aug 21, 2003
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 76528
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG;30MG
Approval Date
Aug 21, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Oct 23, 2002
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40464
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Oct 23, 2002
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;10MG
Approval Date
Oct 23, 2002
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40464
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Oct 23, 2002
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
Oct 25, 2002
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40469
Product No.: 1
Product
Dosage Form: -
Strength: 750MG;7.5MG
Approval Date
Oct 25, 2002
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;10MG
Approval Date
Nov 06, 2002
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40473
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
Nov 06, 2002
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Jan 02, 2003
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40474
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Jan 02, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;10MG
Approval Date
Oct 23, 2002
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40476
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;10MG
Approval Date
Oct 23, 2002
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Nov 06, 2002
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40477
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Nov 06, 2002
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Nov 08, 2002
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40478
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Nov 08, 2002
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;7.5MG
Approval Date
May 21, 2003
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40490
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;7.5MG
Approval Date
May 21, 2003
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;10MG
Approval Date
Aug 16, 2007
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40826
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Aug 16, 2007
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90118
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90118
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Dec 23, 2008
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 90118
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Dec 23, 2008
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Dec 26, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90535
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Dec 26, 2013
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Dec 26, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90535
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Dec 26, 2013
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Dec 26, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90535
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Dec 26, 2013
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Dec 26, 2013
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 90535
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Dec 26, 2013
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;100MG
Approval Date
Jul 11, 2001
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 75838
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Jul 11, 2001
Regulatory Status
Discontinued
Drug Name
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;37.5MG
Approval Date
Dec 16, 2005
Active Ingredient
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Identifiers
Application No.: 77184
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;37.5MG
Approval Date
Dec 16, 2005
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 18337
Product No.: 1
Product
Dosage Form: -
Strength: 650MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 18337
Product No.: 2
Product
Dosage Form: -
Strength: 325MG
Approval Date
Jan 01, 1982
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
120MG
Approval Date
Sep 12, 1983
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 18337
Product No.: 3
Product
Dosage Form: -
Strength: 120MG
Approval Date
Sep 12, 1983
Regulatory Status
OTC
Drug Name
ACETAMINOPHEN AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Jan 02, 2026
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 219053
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Jan 02, 2026
Regulatory Status
OTC
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Jul 01, 2020
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 213046
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Jul 01, 2020
Regulatory Status
RX
Drug Name
INFANTS FEVERALL
Product Number
4
Dosage Form
-
Strength
80MG
Approval Date
Aug 26, 1992
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 18337
Product No.: 4
Product
Dosage Form: -
Strength: 80MG
Approval Date
Aug 26, 1992
Regulatory Status
OTC
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG/15ML;7.5MG/15ML
Approval Date
Dec 30, 2021
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 201295
Product No.: 1
Product
Dosage Form: -
Strength: 325MG/15ML;7.5MG/15ML
Approval Date
Dec 30, 2021
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG/15ML;10MG/15ML
Approval Date
Dec 30, 2021
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 201295
Product No.: 2
Product
Dosage Form: -
Strength: 300MG/15ML;10MG/15ML
Approval Date
Dec 30, 2021
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Mar 27, 2013
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202214
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Mar 27, 2013
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Mar 27, 2013
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202214
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Mar 27, 2013
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Mar 27, 2013
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202214
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Mar 27, 2013
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
300MG;5MG
Approval Date
Mar 15, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202214
Product No.: 4
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Mar 15, 2016
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
5
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Mar 15, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202214
Product No.: 5
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Mar 15, 2016
Regulatory Status
RX
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
6
Dosage Form
-
Strength
300MG;10MG
Approval Date
Mar 15, 2016
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 202214
Product No.: 6
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Mar 15, 2016
Regulatory Status
RX
Drug Name
CO-GESIC
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
May 03, 1982
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 87757
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
May 03, 1982
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
650MG;7.5MG
Approval Date
Nov 21, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40134
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;7.5MG
Approval Date
Nov 21, 1996
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;10MG
Approval Date
Aug 13, 1997
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40210
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
Aug 13, 1997
Regulatory Status
Discontinued
Drug Name
LORTAB
Product Number
1
Dosage Form
-
Strength
500MG;10MG
Approval Date
Jan 26, 1996
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 40100
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;10MG
Approval Date
Jan 26, 1996
Regulatory Status
Discontinued
Drug Name
LORTAB
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jul 09, 1982
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 87722
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jul 09, 1982
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Mar 24, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206484
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Mar 24, 2017
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Mar 24, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206484
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Mar 24, 2017
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Mar 24, 2017
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 206484
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Mar 24, 2017
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85896
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
CAPITAL AND CODEINE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 86024
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
PHRENILIN
Product Number
1
Dosage Form
-
Strength
325MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jun 19, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 87811
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
Jun 19, 1985
Regulatory Status
Discontinued
Drug Name
PHRENILIN FORTE
Product Number
1
Dosage Form
-
Strength
650MG;50MG
Approval Date
Jun 19, 1985
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 88831
Product No.: 1
Product
Dosage Form: -
Strength: 650MG;50MG
Approval Date
Jun 19, 1985
Regulatory Status
Discontinued
Drug Name
PHRENILIN WITH CAFFEINE AND CODEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG;30MG
Approval Date
Aug 22, 2001
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 74911
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG;30MG
Approval Date
Aug 22, 2001
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Mar 16, 2007
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 77677
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Mar 16, 2007
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
650MG;100MG
Approval Date
Mar 16, 2007
Active Ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Identifiers
Application No.: 77677
Product No.: 2
Product
Dosage Form: -
Strength: 650MG;100MG
Approval Date
Mar 16, 2007
Regulatory Status
Discontinued
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;50MG
Approval Date
Aug 23, 2011
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 90956
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG
Approval Date
Aug 23, 2011
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Nov 16, 2009
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 40885
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Nov 16, 2009
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Oct 31, 2018
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 209587
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Oct 31, 2018
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN, CAFFEINE AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG;30MG
Approval Date
Jun 10, 2004
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 76560
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG;30MG
Approval Date
Jun 10, 2004
Regulatory Status
RX
Drug Name
BUTALBITAL, ACETAMINOPHEN, CAFFEINE AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;50MG;40MG;30MG
Approval Date
Jul 19, 2012
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Identifiers
Application No.: 76560
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;50MG;40MG;30MG
Approval Date
Jul 19, 2012
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 87508
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Regulatory Status
RX
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;50MG
Approval Date
Nov 15, 2016
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 207386
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG
Approval Date
Nov 15, 2016
Regulatory Status
RX
Drug Name
ADVIL DUAL ACTION WITH ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Feb 28, 2020
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 211733
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Feb 28, 2020
Regulatory Status
OTC
Drug Name
EXCEDRIN (MIGRAINE RELIEF)
Product Number
1
Dosage Form
-
Strength
250MG;250MG;65MG
Approval Date
Jan 14, 1998
Active Ingredient
ACETAMINOPHEN; ASPIRIN; CAFFEINE
Identifiers
Application No.: 20802
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;250MG;65MG
Approval Date
Jan 14, 1998
Regulatory Status
OTC
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
300MG;50MG;40MG
Approval Date
Aug 04, 2017
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 206615
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG;40MG
Approval Date
Aug 04, 2017
Regulatory Status
Discontinued
Drug Name
TREZIX
Product Number
1
Dosage Form
-
Strength
320.5MG;30MG;16MG
Approval Date
Nov 26, 2014
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Identifiers
Application No.: 204785
Product No.: 1
Product
Dosage Form: -
Strength: 320.5MG;30MG;16MG
Approval Date
Nov 26, 2014
Regulatory Status
Discontinued
Drug Name
APADAZ
Product Number
1
Dosage Form
-
Strength
325MG;EQ 6.12MG BASE
Approval Date
Feb 23, 2018
Active Ingredient
ACETAMINOPHEN; BENZHYDROCODONE HYDROCHLORIDE
Identifiers
Application No.: 208653
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;EQ 6.12MG BASE
Approval Date
Feb 23, 2018
Regulatory Status
Discontinued
Drug Name
APADAZ
Product Number
2
Dosage Form
-
Strength
325MG;EQ 4.08MG BASE
Approval Date
Jan 04, 2019
Active Ingredient
ACETAMINOPHEN; BENZHYDROCODONE HYDROCHLORIDE
Identifiers
Application No.: 208653
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;EQ 4.08MG BASE
Approval Date
Jan 04, 2019
Regulatory Status
Discontinued
Drug Name
APADAZ
Product Number
3
Dosage Form
-
Strength
325MG;EQ 8.16MG BASE
Approval Date
Jan 04, 2019
Active Ingredient
ACETAMINOPHEN; BENZHYDROCODONE HYDROCHLORIDE
Identifiers
Application No.: 208653
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;EQ 8.16MG BASE
Approval Date
Jan 04, 2019
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Oct 21, 2020
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 210969
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Oct 21, 2020
Regulatory Status
RX
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 86366
Product No.: 1
Product
Dosage Form: -
Strength: 120MG/5ML;12MG/5ML
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
250MG;125MG
Approval Date
Jan 17, 2025
Active Ingredient
ACETAMINOPHEN; IBUPROFEN
Identifiers
Application No.: 217241
Product No.: 1
Product
Dosage Form: -
Strength: 250MG;125MG
Approval Date
Jan 17, 2025
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Sep 21, 2020
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 203647
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Sep 21, 2020
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
1GM/100ML (10MG/ML)
Approval Date
Oct 28, 2015
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 204767
Product No.: 1
Product
Dosage Form: -
Strength: 1GM/100ML (10MG/ML)
Approval Date
Oct 28, 2015
Regulatory Status
RX
Drug Name
DHC PLUS
Product Number
1
Dosage Form
-
Strength
356.4MG;30MG;16MG
Approval Date
Mar 04, 1986
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Identifiers
Application No.: 88584
Product No.: 1
Product
Dosage Form: -
Strength: 356.4MG;30MG;16MG
Approval Date
Mar 04, 1986
Regulatory Status
Discontinued
Drug Name
PROVAL #3
Product Number
1
Dosage Form
-
Strength
325MG;30MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Identifiers
Application No.: 85685
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;30MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
NEOPAP
Product Number
1
Dosage Form
-
Strength
120MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN
Identifiers
Application No.: 16401
Product No.: 1
Product
Dosage Form: -
Strength: 120MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
Dec 30, 2021
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 214928
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Dec 30, 2021
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Dec 30, 2021
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 214928
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Dec 30, 2021
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
Dec 30, 2021
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 214928
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Dec 30, 2021
Regulatory Status
Discontinued
Drug Name
ANOQUAN
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Oct 01, 1986
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 87628
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Oct 01, 1986
Regulatory Status
Discontinued
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;50MG
Approval Date
Oct 30, 2015
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 205120
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG
Approval Date
Oct 30, 2015
Regulatory Status
Discontinued
Drug Name
BUTALBITAL AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;50MG
Approval Date
Jun 05, 2017
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Identifiers
Application No.: 207635
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;50MG
Approval Date
Jun 05, 2017
Regulatory Status
Discontinued
Drug Name
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG
Approval Date
Jan 10, 2017
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Identifiers
Application No.: 204984
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;50MG;40MG
Approval Date
Jan 10, 2017
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
300MG;5MG
Approval Date
Nov 08, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 208540
Product No.: 1
Product
Dosage Form: -
Strength: 300MG;5MG
Approval Date
Nov 08, 2018
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
300MG;7.5MG
Approval Date
Nov 08, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 208540
Product No.: 2
Product
Dosage Form: -
Strength: 300MG;7.5MG
Approval Date
Nov 08, 2018
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
300MG;10MG
Approval Date
Nov 08, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 208540
Product No.: 3
Product
Dosage Form: -
Strength: 300MG;10MG
Approval Date
Nov 08, 2018
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;2.5MG
Approval Date
Oct 24, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209958
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;2.5MG
Approval Date
Oct 24, 2018
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;5MG
Approval Date
Oct 24, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209958
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Oct 24, 2018
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Oct 24, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209958
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Oct 24, 2018
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
4
Dosage Form
-
Strength
325MG;10MG
Approval Date
Oct 24, 2018
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 209958
Product No.: 4
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Oct 24, 2018
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
Jul 26, 2012
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 202677
Product No.: 1
Product
Dosage Form: -
Strength: 325MG;7.5MG
Approval Date
Jul 26, 2012
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;10MG
Approval Date
Jul 26, 2012
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 202677
Product No.: 2
Product
Dosage Form: -
Strength: 325MG;10MG
Approval Date
Jul 26, 2012
Regulatory Status
RX
Drug Name
OXYCODONE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;5MG
Approval Date
Mar 08, 2016
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 202677
Product No.: 3
Product
Dosage Form: -
Strength: 325MG;5MG
Approval Date
Mar 08, 2016
Regulatory Status
RX
Drug Name
OXYCODONE 2.5/APAP 500
Product Number
1
Dosage Form
-
Strength
500MG;2.5MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 85910
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;2.5MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
Drug Name
OXYCODONE 5/APAP 500
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
Jan 01, 1982
Active Ingredient
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Identifiers
Application No.: 85911
Product No.: 1
Product
Dosage Form: -
Strength: 500MG;5MG
Approval Date
Jan 01, 1982
Regulatory Status
Discontinued
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Related Databases
5 of 6 have recordsDrug Status Breakdown
739 total- Discontinued
- RX
- OTC
- Unclassified
Official Source
FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.
Visit FDA Orange BookRecord Details Preview
Click "View Details" on any record above to expand full details inline.
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Identifiers
Application No.: 85667
Product No.: 1
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