Upsher-Smith Laboratories Discontinued
FDA Approved Drugs
Upsher-Smith Laboratories Discontinued
FDA Approved Drugs Database
FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.
- Total Records 75
- Latest Approval Date Jan 22, 2026
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Company
Upsher-Smith Laboratories Discontinued
Country
U.S.A
Website
Social Profiles
Company Snapshot
Upsher-Smith Laboratories Discontinued
Upsher-Smith Laboratories, Inc., 6701 Evenstad Drive, Maple Grove, MN 55369
U.S.A
www.upsher-smith.com/ uslinfo@upsher-smith.com View on MapFDA Approved Drug Records ( 75 records )
Drug Name
AMIODARONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1998-12-23
Active Ingredient
AMIODARONE HYDROCHLORIDE
Application Number
75315
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1998-12-23
Regulatory Status
Discontinued
Drug Name
AMIODARONE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
400MG
Approval Date
2000-06-30
Active Ingredient
AMIODARONE HYDROCHLORIDE
Application Number
75315
Product Number
2
Dosage Form
-
Strength
400MG
Approval Date
2000-06-30
Regulatory Status
Discontinued
Drug Name
BRIMONIDINE TARTRATE
Product Number
1
Dosage Form
-
Strength
0.15%
Approval Date
2024-06-12
Active Ingredient
BRIMONIDINE TARTRATE
Application Number
216772
Product Number
1
Dosage Form
-
Strength
0.15%
Approval Date
2024-06-12
Regulatory Status
Discontinued
Drug Name
BRIMONIDINE TARTRATE
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
2025-07-30
Active Ingredient
BRIMONIDINE TARTRATE
Application Number
217599
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
2025-07-30
Regulatory Status
Discontinued
Drug Name
BROMPHENIRAMINE MALEATE
Product Number
1
Dosage Form
-
Strength
4MG
Approval Date
1982-01-01
Active Ingredient
BROMPHENIRAMINE MALEATE
Application Number
83215
Product Number
1
Dosage Form
-
Strength
4MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORDIAZEPOXIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE HYDROCHLORIDE
Application Number
84823
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORDIAZEPOXIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE HYDROCHLORIDE
Application Number
84919
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORDIAZEPOXIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE HYDROCHLORIDE
Application Number
84920
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CIMETIDINE
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1996-01-24
Active Ingredient
CIMETIDINE
Application Number
74506
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1996-01-24
Regulatory Status
Discontinued
Drug Name
CIMETIDINE
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
1996-01-24
Active Ingredient
CIMETIDINE
Application Number
74506
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
1996-01-24
Regulatory Status
Discontinued
Drug Name
CIMETIDINE
Product Number
3
Dosage Form
-
Strength
400MG
Approval Date
1996-01-24
Active Ingredient
CIMETIDINE
Application Number
74506
Product Number
3
Dosage Form
-
Strength
400MG
Approval Date
1996-01-24
Regulatory Status
Discontinued
Drug Name
CIMETIDINE
Product Number
4
Dosage Form
-
Strength
800MG
Approval Date
1996-01-24
Active Ingredient
CIMETIDINE
Application Number
74506
Product Number
4
Dosage Form
-
Strength
800MG
Approval Date
1996-01-24
Regulatory Status
Discontinued
Drug Name
CLOBAZAM
Product Number
1
Dosage Form
-
Strength
2.5MG/ML
Approval Date
2018-10-22
Active Ingredient
CLOBAZAM
Application Number
210569
Product Number
1
Dosage Form
-
Strength
2.5MG/ML
Approval Date
2018-10-22
Regulatory Status
Discontinued
Drug Name
DEXAMETHASONE
Product Number
1
Dosage Form
-
Strength
1.5MG
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE
Application Number
87533
Product Number
1
Dosage Form
-
Strength
1.5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXAMETHASONE
Product Number
1
Dosage Form
-
Strength
0.75MG
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE
Application Number
87534
Product Number
1
Dosage Form
-
Strength
0.75MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DROXIDOPA
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
2021-02-18
Active Ingredient
DROXIDOPA
Application Number
213661
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
2021-02-18
Regulatory Status
Discontinued
Drug Name
DROXIDOPA
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
2021-02-18
Active Ingredient
DROXIDOPA
Application Number
213661
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
2021-02-18
Regulatory Status
Discontinued
Drug Name
DROXIDOPA
Product Number
3
Dosage Form
-
Strength
300MG
Approval Date
2021-02-18
Active Ingredient
DROXIDOPA
Application Number
213661
Product Number
3
Dosage Form
-
Strength
300MG
Approval Date
2021-02-18
Regulatory Status
Discontinued
Drug Name
FLUOXYMESTERONE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1983-10-21
Active Ingredient
FLUOXYMESTERONE
Application Number
88342
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1983-10-21
Regulatory Status
Discontinued
Drug Name
FLUVOXAMINE MALEATE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2001-01-05
Active Ingredient
FLUVOXAMINE MALEATE
Application Number
75887
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2001-01-05
Regulatory Status
Discontinued
Drug Name
FLUVOXAMINE MALEATE
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2001-01-05
Active Ingredient
FLUVOXAMINE MALEATE
Application Number
75887
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2001-01-05
Regulatory Status
Discontinued
Drug Name
FLUVOXAMINE MALEATE
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2001-01-05
Active Ingredient
FLUVOXAMINE MALEATE
Application Number
75887
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2001-01-05
Regulatory Status
Discontinued
Drug Name
FORTICAL
Product Number
1
Dosage Form
-
Strength
200 IU/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2005-08-12
Active Ingredient
CALCITONIN SALMON RECOMBINANT
Application Number
21406
Product Number
1
Dosage Form
-
Strength
200 IU/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2005-08-12
Regulatory Status
Discontinued
Drug Name
FOSINOPRIL SODIUM
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2004-10-08
Active Ingredient
FOSINOPRIL SODIUM
Application Number
76188
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2004-10-08
Regulatory Status
Discontinued
Drug Name
FOSINOPRIL SODIUM
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
2004-10-08
Active Ingredient
FOSINOPRIL SODIUM
Application Number
76188
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
2004-10-08
Regulatory Status
Discontinued
Drug Name
FOSINOPRIL SODIUM
Product Number
3
Dosage Form
-
Strength
40MG
Approval Date
2004-10-08
Active Ingredient
FOSINOPRIL SODIUM
Application Number
76188
Product Number
3
Dosage Form
-
Strength
40MG
Approval Date
2004-10-08
Regulatory Status
Discontinued
Drug Name
GLUTETHIMIDE
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
GLUTETHIMIDE
Application Number
83234
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDRALAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
HYDRALAZINE HYDROCHLORIDE
Application Number
83241
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDRALAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
HYDRALAZINE HYDROCHLORIDE
Application Number
83560
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDRALAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Active Ingredient
HYDRALAZINE HYDROCHLORIDE
Application Number
83561
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDRALAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Active Ingredient
HYDRALAZINE HYDROCHLORIDE
Application Number
85088
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
2017-03-24
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
206484
Product Number
1
Dosage Form
-
Strength
325MG;5MG
Approval Date
2017-03-24
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
2017-03-24
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
206484
Product Number
2
Dosage Form
-
Strength
325MG;7.5MG
Approval Date
2017-03-24
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
2017-03-24
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
206484
Product Number
3
Dosage Form
-
Strength
325MG;10MG
Approval Date
2017-03-24
Regulatory Status
Discontinued
Drug Name
KLOR-CON
Product Number
1
Dosage Form
-
Strength
8MEQ
Approval Date
2015-07-10
Active Ingredient
POTASSIUM CHLORIDE
Application Number
203106
Product Number
1
Dosage Form
-
Strength
8MEQ
Approval Date
2015-07-10
Regulatory Status
Discontinued
Drug Name
KLOR-CON
Product Number
2
Dosage Form
-
Strength
10MEQ
Approval Date
2015-07-10
Active Ingredient
POTASSIUM CHLORIDE
Application Number
203106
Product Number
2
Dosage Form
-
Strength
10MEQ
Approval Date
2015-07-10
Regulatory Status
Discontinued
Drug Name
MEDROXYPROGESTERONE ACETATE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1984-07-26
Active Ingredient
MEDROXYPROGESTERONE ACETATE
Application Number
88484
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1984-07-26
Regulatory Status
Discontinued
Drug Name
METHOCARBAMOL
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
METHOCARBAMOL
Application Number
87453
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
METHOCARBAMOL
Product Number
1
Dosage Form
-
Strength
750MG
Approval Date
1982-01-01
Active Ingredient
METHOCARBAMOL
Application Number
87454
Product Number
1
Dosage Form
-
Strength
750MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MIRTAZAPINE
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
2003-06-19
Active Ingredient
MIRTAZAPINE
Application Number
76189
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
2003-06-19
Regulatory Status
Discontinued
Drug Name
MIRTAZAPINE
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
2003-06-19
Active Ingredient
MIRTAZAPINE
Application Number
76189
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
2003-06-19
Regulatory Status
Discontinued
Drug Name
MIRTAZAPINE
Product Number
3
Dosage Form
-
Strength
45MG
Approval Date
2003-06-19
Active Ingredient
MIRTAZAPINE
Application Number
76189
Product Number
3
Dosage Form
-
Strength
45MG
Approval Date
2003-06-19
Regulatory Status
Discontinued
Drug Name
OSELTAMIVIR PHOSPHATE
Product Number
1
Dosage Form
-
Strength
EQ 30MG BASE
Approval Date
2026-01-22
Active Ingredient
OSELTAMIVIR PHOSPHATE
Application Number
213437
Product Number
1
Dosage Form
-
Strength
EQ 30MG BASE
Approval Date
2026-01-22
Regulatory Status
Discontinued
Drug Name
OSELTAMIVIR PHOSPHATE
Product Number
2
Dosage Form
-
Strength
EQ 45MG BASE
Approval Date
2026-01-22
Active Ingredient
OSELTAMIVIR PHOSPHATE
Application Number
213437
Product Number
2
Dosage Form
-
Strength
EQ 45MG BASE
Approval Date
2026-01-22
Regulatory Status
Discontinued
Drug Name
OSELTAMIVIR PHOSPHATE
Product Number
3
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2026-01-22
Active Ingredient
OSELTAMIVIR PHOSPHATE
Application Number
213437
Product Number
3
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2026-01-22
Regulatory Status
Discontinued
Drug Name
OXANDROLONE
Product Number
1
Dosage Form
-
Strength
2.5MG
Approval Date
2006-12-01
Active Ingredient
OXANDROLONE
Application Number
76761
Product Number
1
Dosage Form
-
Strength
2.5MG
Approval Date
2006-12-01
Regulatory Status
Discontinued
Drug Name
OXANDROLONE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2007-03-22
Active Ingredient
OXANDROLONE
Application Number
78033
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2007-03-22
Regulatory Status
Discontinued
Drug Name
PAROXETINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
2004-03-08
Active Ingredient
PAROXETINE HYDROCHLORIDE
Application Number
75566
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
2004-03-08
Regulatory Status
Discontinued
Drug Name
PAROXETINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE
Approval Date
2004-03-08
Active Ingredient
PAROXETINE HYDROCHLORIDE
Application Number
75566
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE
Approval Date
2004-03-08
Regulatory Status
Discontinued
Drug Name
PAROXETINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
EQ 30MG BASE
Approval Date
2004-03-08
Active Ingredient
PAROXETINE HYDROCHLORIDE
Application Number
75566
Product Number
3
Dosage Form
-
Strength
EQ 30MG BASE
Approval Date
2004-03-08
Regulatory Status
Discontinued
Drug Name
PAROXETINE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
EQ 40MG BASE
Approval Date
2004-03-08
Active Ingredient
PAROXETINE HYDROCHLORIDE
Application Number
75566
Product Number
4
Dosage Form
-
Strength
EQ 40MG BASE
Approval Date
2004-03-08
Regulatory Status
Discontinued
Drug Name
PENTOXIL
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1999-03-31
Active Ingredient
PENTOXIFYLLINE
Application Number
74962
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1999-03-31
Regulatory Status
Discontinued
Drug Name
PHENDIMETRAZINE TARTRATE
Product Number
1
Dosage Form
-
Strength
35MG
Approval Date
1982-01-01
Active Ingredient
PHENDIMETRAZINE TARTRATE
Application Number
84399
Product Number
1
Dosage Form
-
Strength
35MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PHENTERMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
1982-04-09
Active Ingredient
PHENTERMINE HYDROCHLORIDE
Application Number
84487
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
1982-04-09
Regulatory Status
Discontinued
Drug Name
PHENTERMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
1984-03-27
Active Ingredient
PHENTERMINE HYDROCHLORIDE
Application Number
88430
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
1984-03-27
Regulatory Status
Discontinued
Drug Name
PREDNISONE
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1982-01-01
Active Ingredient
PREDNISONE
Application Number
87470
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PREDNISONE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Active Ingredient
PREDNISONE
Application Number
87471
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
60MG
Approval Date
2009-03-06
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
78311
Product Number
1
Dosage Form
-
Strength
60MG
Approval Date
2009-03-06
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
80MG
Approval Date
2009-03-06
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
78311
Product Number
2
Dosage Form
-
Strength
80MG
Approval Date
2009-03-06
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
120MG
Approval Date
2009-03-06
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
78311
Product Number
3
Dosage Form
-
Strength
120MG
Approval Date
2009-03-06
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
160MG
Approval Date
2009-03-06
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
78311
Product Number
4
Dosage Form
-
Strength
160MG
Approval Date
2009-03-06
Regulatory Status
Discontinued
Drug Name
SOTALOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
2000-05-01
Active Ingredient
SOTALOL HYDROCHLORIDE
Application Number
75366
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
2000-05-01
Regulatory Status
Discontinued
Drug Name
SOTALOL HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
120MG
Approval Date
2000-05-01
Active Ingredient
SOTALOL HYDROCHLORIDE
Application Number
75366
Product Number
2
Dosage Form
-
Strength
120MG
Approval Date
2000-05-01
Regulatory Status
Discontinued
Drug Name
SOTALOL HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
160MG
Approval Date
2000-05-01
Active Ingredient
SOTALOL HYDROCHLORIDE
Application Number
75366
Product Number
3
Dosage Form
-
Strength
160MG
Approval Date
2000-05-01
Regulatory Status
Discontinued
Drug Name
SOTALOL HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
240MG
Approval Date
2000-05-01
Active Ingredient
SOTALOL HYDROCHLORIDE
Application Number
75366
Product Number
4
Dosage Form
-
Strength
240MG
Approval Date
2000-05-01
Regulatory Status
Discontinued
Drug Name
SPIRONOLACTONE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
SPIRONOLACTONE
Application Number
87554
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
25MG;25MG
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE; SPIRONOLACTONE
Application Number
87553
Product Number
1
Dosage Form
-
Strength
25MG;25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TROSPIUM CHLORIDE
Product Number
1
Dosage Form
-
Strength
60MG
Approval Date
2015-04-29
Active Ingredient
TROSPIUM CHLORIDE
Application Number
91635
Product Number
1
Dosage Form
-
Strength
60MG
Approval Date
2015-04-29
Regulatory Status
Discontinued
Drug Name
ZALEPLON
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2008-06-06
Active Ingredient
ZALEPLON
Application Number
78095
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2008-06-06
Regulatory Status
Discontinued
Drug Name
ZALEPLON
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2008-06-06
Active Ingredient
ZALEPLON
Application Number
78095
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2008-06-06
Regulatory Status
Discontinued
Drug Name
ZALEPLON
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2008-06-06
Active Ingredient
ZALEPLON
Application Number
78706
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2008-06-06
Regulatory Status
Discontinued
Drug Name
ZALEPLON
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2008-06-06
Active Ingredient
ZALEPLON
Application Number
78706
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2008-06-06
Regulatory Status
Discontinued
Drug Name
ZONISAMIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2005-12-22
Active Ingredient
ZONISAMIDE
Application Number
77644
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2005-12-22
Regulatory Status
Discontinued
Drug Name
ZONISAMIDE
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2005-12-22
Active Ingredient
ZONISAMIDE
Application Number
77644
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2005-12-22
Regulatory Status
Discontinued
Drug Name
ZONISAMIDE
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2005-12-22
Active Ingredient
ZONISAMIDE
Application Number
77644
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2005-12-22
Regulatory Status
Discontinued
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Drug Status Breakdown
75 total- Discontinued
Official Source
FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.
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Explore important FDA approved drug information available in the records above.
Drug Name
AMIODARONE HYDROCHLORIDE
Application Number
75315
Product Number
1
Active Ingredient
AMIODARONE HYDROCHLORIDE
Dosage Form
-
Strength
200MG
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