Merck & Co Discontinued
FDA Approved Drugs
Merck & Co 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 125
- Latest Approval Date Jan 25, 2008
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Social Profiles
Company Snapshot
Merck & Co Discontinued
One Merck Drive, P.O. Box 100 Whitehouse Station, NJ 08889-0100
U.S.A
www.merck.com/ View on MapFDA Approved Drug Records ( 125 records )
Drug Name
AFRINOL
Product Number
1
Dosage Form
-
Strength
120MG
Approval Date
1982-01-01
Active Ingredient
PSEUDOEPHEDRINE SULFATE
Application Number
18191
Product Number
1
Dosage Form
-
Strength
120MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDOCLOR-150
Product Number
1
Dosage Form
-
Strength
150MG;250MG
Approval Date
1982-01-01
Active Ingredient
CHLOROTHIAZIDE; METHYLDOPA
Application Number
16016
Product Number
1
Dosage Form
-
Strength
150MG;250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDOCLOR-250
Product Number
2
Dosage Form
-
Strength
250MG;250MG
Approval Date
1982-01-01
Active Ingredient
CHLOROTHIAZIDE; METHYLDOPA
Application Number
16016
Product Number
2
Dosage Form
-
Strength
250MG;250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDOMET
Product Number
1
Dosage Form
-
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
METHYLDOPA
Application Number
13400
Product Number
1
Dosage Form
-
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDOMET
Product Number
2
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
METHYLDOPA
Application Number
13400
Product Number
2
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDOMET
Product Number
3
Dosage Form
-
Strength
125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
METHYLDOPA
Application Number
13400
Product Number
3
Dosage Form
-
Strength
125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDOMET
Product Number
1
Dosage Form
-
Strength
50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
METHYLDOPATE HYDROCHLORIDE
Application Number
13401
Product Number
1
Dosage Form
-
Strength
50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDOMET
Product Number
1
Dosage Form
-
Strength
250MG/5ML
Approval Date
1982-01-01
Active Ingredient
METHYLDOPA
Application Number
18389
Product Number
1
Dosage Form
-
Strength
250MG/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDORIL 15
Product Number
1
Dosage Form
-
Strength
15MG;250MG
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE; METHYLDOPA
Application Number
13402
Product Number
1
Dosage Form
-
Strength
15MG;250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDORIL 25
Product Number
2
Dosage Form
-
Strength
25MG;250MG
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE; METHYLDOPA
Application Number
13402
Product Number
2
Dosage Form
-
Strength
25MG;250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDORIL D30
Product Number
3
Dosage Form
-
Strength
30MG;500MG
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE; METHYLDOPA
Application Number
13402
Product Number
3
Dosage Form
-
Strength
30MG;500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALDORIL D50
Product Number
4
Dosage Form
-
Strength
50MG;500MG
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE; METHYLDOPA
Application Number
13402
Product Number
4
Dosage Form
-
Strength
50MG;500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALPHAREDISOL
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
1982-01-01
Active Ingredient
HYDROXOCOBALAMIN
Application Number
80778
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
AMINOHIPPURATE SODIUM
Product Number
1
Dosage Form
-
Strength
20%
Approval Date
1982-01-01
Active Ingredient
AMINOHIPPURATE SODIUM
Application Number
5619
Product Number
1
Dosage Form
-
Strength
20%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ARAMINE
Product Number
2
Dosage Form
-
Strength
EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-12-22
Active Ingredient
METARAMINOL BITARTRATE
Application Number
9509
Product Number
2
Dosage Form
-
Strength
EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-12-22
Regulatory Status
Discontinued
Drug Name
BENEMID
Product Number
4
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
PROBENECID
Application Number
7898
Product Number
4
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BLOCADREN
Product Number
1
Dosage Form
-
Strength
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
TIMOLOL MALEATE
Application Number
18017
Product Number
1
Dosage Form
-
Strength
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BLOCADREN
Product Number
2
Dosage Form
-
Strength
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
TIMOLOL MALEATE
Application Number
18017
Product Number
2
Dosage Form
-
Strength
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BLOCADREN
Product Number
4
Dosage Form
-
Strength
20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
TIMOLOL MALEATE
Application Number
18017
Product Number
4
Dosage Form
-
Strength
20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CANCIDAS
Product Number
1
Dosage Form
-
Strength
50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2001-01-26
Active Ingredient
CASPOFUNGIN ACETATE
Application Number
21227
Product Number
1
Dosage Form
-
Strength
50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2001-01-26
Regulatory Status
Discontinued
Drug Name
CANCIDAS
Product Number
2
Dosage Form
-
Strength
70MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2001-01-26
Active Ingredient
CASPOFUNGIN ACETATE
Application Number
21227
Product Number
2
Dosage Form
-
Strength
70MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2001-01-26
Regulatory Status
Discontinued
Drug Name
CHIBROXIN
Product Number
1
Dosage Form
-
Strength
0.3%
Approval Date
1991-06-17
Active Ingredient
NORFLOXACIN
Application Number
19757
Product Number
1
Dosage Form
-
Strength
0.3%
Approval Date
1991-06-17
Regulatory Status
Discontinued
Drug Name
CHLOR-TRIMETON
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1982-01-01
Active Ingredient
CHLORPHENIRAMINE MALEATE
Application Number
8794
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLOR-TRIMETON
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1982-01-01
Active Ingredient
CHLORPHENIRAMINE MALEATE
Application Number
8826
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CLINORIL
Product Number
1
Dosage Form
-
Strength
150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
SULINDAC
Application Number
17911
Product Number
1
Dosage Form
-
Strength
150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CLINORIL
Product Number
2
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
SULINDAC
Application Number
17911
Product Number
2
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
COGENTIN
Product Number
2
Dosage Form
-
Strength
2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
BENZTROPINE MESYLATE
Application Number
9193
Product Number
2
Dosage Form
-
Strength
2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
COGENTIN
Product Number
3
Dosage Form
-
Strength
1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
BENZTROPINE MESYLATE
Application Number
9193
Product Number
3
Dosage Form
-
Strength
1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
COGENTIN
Product Number
4
Dosage Form
-
Strength
0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
BENZTROPINE MESYLATE
Application Number
9193
Product Number
4
Dosage Form
-
Strength
0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
COLBENEMID
Product Number
1
Dosage Form
-
Strength
0.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
COLCHICINE; PROBENECID
Application Number
12383
Product Number
1
Dosage Form
-
Strength
0.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CORTONE
Product Number
2
Dosage Form
-
Strength
25MG/ML
Approval Date
1982-01-01
Active Ingredient
CORTISONE ACETATE
Application Number
7110
Product Number
2
Dosage Form
-
Strength
25MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CORTONE
Product Number
3
Dosage Form
-
Strength
50MG/ML
Approval Date
1982-01-01
Active Ingredient
CORTISONE ACETATE
Application Number
7110
Product Number
3
Dosage Form
-
Strength
50MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CORTONE
Product Number
3
Dosage Form
-
Strength
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CORTISONE ACETATE
Application Number
7750
Product Number
3
Dosage Form
-
Strength
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CYCLAINE
Product Number
1
Dosage Form
-
Strength
5%
Approval Date
1982-01-01
Active Ingredient
HEXYLCAINE HYDROCHLORIDE
Application Number
8472
Product Number
1
Dosage Form
-
Strength
5%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADERM
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE
Application Number
13538
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
1
Dosage Form
-
Strength
0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE
Application Number
11664
Product Number
1
Dosage Form
-
Strength
0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
2
Dosage Form
-
Strength
0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE
Application Number
11664
Product Number
2
Dosage Form
-
Strength
0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
3
Dosage Form
-
Strength
1.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE
Application Number
11664
Product Number
3
Dosage Form
-
Strength
1.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
4
Dosage Form
-
Strength
0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE
Application Number
11664
Product Number
4
Dosage Form
-
Strength
0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
5
Dosage Form
-
Strength
4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE
Application Number
11664
Product Number
5
Dosage Form
-
Strength
4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
6
Dosage Form
-
Strength
6MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-07-30
Active Ingredient
DEXAMETHASONE
Application Number
11664
Product Number
6
Dosage Form
-
Strength
6MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-07-30
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
1
Dosage Form
-
Strength
EQ 0.05% PHOSPHATE
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE SODIUM PHOSPHATE
Application Number
11977
Product Number
1
Dosage Form
-
Strength
EQ 0.05% PHOSPHATE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
2
Dosage Form
-
Strength
EQ 0.1% PHOSPHATE
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE SODIUM PHOSPHATE
Application Number
11983
Product Number
2
Dosage Form
-
Strength
EQ 0.1% PHOSPHATE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
1
Dosage Form
-
Strength
EQ 0.1% PHOSPHATE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE SODIUM PHOSPHATE
Application Number
11984
Product Number
1
Dosage Form
-
Strength
EQ 0.1% PHOSPHATE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
2
Dosage Form
-
Strength
EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE SODIUM PHOSPHATE
Application Number
12071
Product Number
2
Dosage Form
-
Strength
EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
4
Dosage Form
-
Strength
EQ 24MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE SODIUM PHOSPHATE
Application Number
12071
Product Number
4
Dosage Form
-
Strength
EQ 24MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON
Product Number
2
Dosage Form
-
Strength
0.5MG/5ML
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE
Application Number
12376
Product Number
2
Dosage Form
-
Strength
0.5MG/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON W/ XYLOCAINE
Product Number
2
Dosage Form
-
Strength
EQ 4MG PHOSPHATE/ML;10MG/ML
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE SODIUM PHOSPHATE; LIDOCAINE HYDROCHLORIDE
Application Number
13334
Product Number
2
Dosage Form
-
Strength
EQ 4MG PHOSPHATE/ML;10MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECADRON-LA
Product Number
1
Dosage Form
-
Strength
EQ 8MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE ACETATE
Application Number
16675
Product Number
1
Dosage Form
-
Strength
EQ 8MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DECASPRAY
Product Number
2
Dosage Form
-
Strength
0.04% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE
Application Number
12731
Product Number
2
Dosage Form
-
Strength
0.04% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DISOPHROL
Product Number
4
Dosage Form
-
Strength
6MG;120MG
Approval Date
1982-09-13
Active Ingredient
DEXBROMPHENIRAMINE MALEATE; PSEUDOEPHEDRINE SULFATE
Application Number
13483
Product Number
4
Dosage Form
-
Strength
6MG;120MG
Approval Date
1982-09-13
Regulatory Status
Discontinued
Drug Name
DIUPRES-250
Product Number
3
Dosage Form
-
Strength
250MG;0.125MG
Approval Date
1987-08-26
Active Ingredient
CHLOROTHIAZIDE; RESERPINE
Application Number
11635
Product Number
3
Dosage Form
-
Strength
250MG;0.125MG
Approval Date
1987-08-26
Regulatory Status
Discontinued
Drug Name
DIUPRES-500
Product Number
6
Dosage Form
-
Strength
500MG;0.125MG
Approval Date
1987-08-26
Active Ingredient
CHLOROTHIAZIDE; RESERPINE
Application Number
11635
Product Number
6
Dosage Form
-
Strength
500MG;0.125MG
Approval Date
1987-08-26
Regulatory Status
Discontinued
Drug Name
DOLOBID
Product Number
1
Dosage Form
-
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-04-19
Active Ingredient
DIFLUNISAL
Application Number
18445
Product Number
1
Dosage Form
-
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-04-19
Regulatory Status
Discontinued
Drug Name
DOLOBID
Product Number
2
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-04-19
Active Ingredient
DIFLUNISAL
Application Number
18445
Product Number
2
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-04-19
Regulatory Status
Discontinued
Drug Name
DRIXORAL
Product Number
3
Dosage Form
-
Strength
6MG;120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-09-13
Active Ingredient
DEXBROMPHENIRAMINE MALEATE; PSEUDOEPHEDRINE SULFATE
Application Number
13483
Product Number
3
Dosage Form
-
Strength
6MG;120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-09-13
Regulatory Status
Discontinued
Drug Name
DRIXORAL PLUS
Product Number
1
Dosage Form
-
Strength
500MG;3MG;60MG
Approval Date
1987-05-22
Active Ingredient
ACETAMINOPHEN; DEXBROMPHENIRAMINE MALEATE; PSEUDOEPHEDRINE SULFATE
Application Number
19453
Product Number
1
Dosage Form
-
Strength
500MG;3MG;60MG
Approval Date
1987-05-22
Regulatory Status
Discontinued
Drug Name
EMEND
Product Number
1
Dosage Form
-
Strength
EQ 115MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2008-01-25
Active Ingredient
FOSAPREPITANT DIMEGLUMINE
Application Number
22023
Product Number
1
Dosage Form
-
Strength
EQ 115MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2008-01-25
Regulatory Status
Discontinued
Drug Name
FLOROPRYL
Product Number
1
Dosage Form
-
Strength
0.025%
Approval Date
1982-01-01
Active Ingredient
ISOFLUROPHATE
Application Number
10656
Product Number
1
Dosage Form
-
Strength
0.025%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
FOSAMAX
Product Number
1
Dosage Form
-
Strength
EQ 70MG BASE/75ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-09-17
Active Ingredient
ALENDRONATE SODIUM
Application Number
21575
Product Number
1
Dosage Form
-
Strength
EQ 70MG BASE/75ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-09-17
Regulatory Status
Discontinued
Drug Name
HUMORSOL
Product Number
1
Dosage Form
-
Strength
0.25%
Approval Date
1982-01-01
Active Ingredient
DEMECARIUM BROMIDE
Application Number
11860
Product Number
1
Dosage Form
-
Strength
0.25%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HUMORSOL
Product Number
2
Dosage Form
-
Strength
0.125%
Approval Date
1982-01-01
Active Ingredient
DEMECARIUM BROMIDE
Application Number
11860
Product Number
2
Dosage Form
-
Strength
0.125%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDELTRA-TBA
Product Number
1
Dosage Form
-
Strength
20MG/ML
Approval Date
1982-01-01
Active Ingredient
PREDNISOLONE TEBUTATE
Application Number
10562
Product Number
1
Dosage Form
-
Strength
20MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDELTRASOL
Product Number
1
Dosage Form
-
Strength
EQ 0.25% PHOSPHATE
Approval Date
1982-01-01
Active Ingredient
PREDNISOLONE SODIUM PHOSPHATE
Application Number
11028
Product Number
1
Dosage Form
-
Strength
EQ 0.25% PHOSPHATE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDELTRASOL
Product Number
2
Dosage Form
-
Strength
EQ 20MG PHOSPHATE/ML
Approval Date
1982-01-01
Active Ingredient
PREDNISOLONE SODIUM PHOSPHATE
Application Number
11583
Product Number
2
Dosage Form
-
Strength
EQ 20MG PHOSPHATE/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCORTONE
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE ACETATE
Application Number
8228
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCORTONE
Product Number
4
Dosage Form
-
Strength
50MG/ML
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE ACETATE
Application Number
8228
Product Number
4
Dosage Form
-
Strength
50MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCORTONE
Product Number
7
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE
Application Number
8506
Product Number
7
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCORTONE
Product Number
11
Dosage Form
-
Strength
20MG
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE
Application Number
8506
Product Number
11
Dosage Form
-
Strength
20MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCORTONE
Product Number
3
Dosage Form
-
Strength
1.5%
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE ACETATE
Application Number
9018
Product Number
3
Dosage Form
-
Strength
1.5%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCORTONE
Product Number
1
Dosage Form
-
Strength
EQ 50MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE SODIUM PHOSPHATE
Application Number
12052
Product Number
1
Dosage Form
-
Strength
EQ 50MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDRODIURIL
Product Number
3
Dosage Form
-
Strength
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE
Application Number
11835
Product Number
3
Dosage Form
-
Strength
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDRODIURIL
Product Number
6
Dosage Form
-
Strength
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE
Application Number
11835
Product Number
6
Dosage Form
-
Strength
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDRODIURIL
Product Number
7
Dosage Form
-
Strength
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE
Application Number
11835
Product Number
7
Dosage Form
-
Strength
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROPRES 25
Product Number
2
Dosage Form
-
Strength
25MG;0.125MG
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE; RESERPINE
Application Number
11958
Product Number
2
Dosage Form
-
Strength
25MG;0.125MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROPRES 50
Product Number
3
Dosage Form
-
Strength
50MG;0.125MG
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE; RESERPINE
Application Number
11958
Product Number
3
Dosage Form
-
Strength
50MG;0.125MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
IMDUR
Product Number
1
Dosage Form
-
Strength
30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-08-12
Active Ingredient
ISOSORBIDE MONONITRATE
Application Number
20225
Product Number
1
Dosage Form
-
Strength
30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-08-12
Regulatory Status
Discontinued
Drug Name
IMDUR
Product Number
2
Dosage Form
-
Strength
60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-08-12
Active Ingredient
ISOSORBIDE MONONITRATE
Application Number
20225
Product Number
2
Dosage Form
-
Strength
60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-08-12
Regulatory Status
Discontinued
Drug Name
IMDUR
Product Number
3
Dosage Form
-
Strength
120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-03-30
Active Ingredient
ISOSORBIDE MONONITRATE
Application Number
20225
Product Number
3
Dosage Form
-
Strength
120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-03-30
Regulatory Status
Discontinued
Drug Name
LERITINE
Product Number
3
Dosage Form
-
Strength
25MG/ML
Approval Date
1982-01-01
Active Ingredient
ANILERIDINE PHOSPHATE
Application Number
10520
Product Number
3
Dosage Form
-
Strength
25MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LERITINE
Product Number
2
Dosage Form
-
Strength
EQ 25MG BASE
Approval Date
1982-01-01
Active Ingredient
ANILERIDINE HYDROCHLORIDE
Application Number
10585
Product Number
2
Dosage Form
-
Strength
EQ 25MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LOTRIMIN
Product Number
1
Dosage Form
-
Strength
1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CLOTRIMAZOLE
Application Number
17613
Product Number
1
Dosage Form
-
Strength
1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LOTRIMIN
Product Number
1
Dosage Form
-
Strength
1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CLOTRIMAZOLE
Application Number
17619
Product Number
1
Dosage Form
-
Strength
1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MANNITOL 25%
Product Number
1
Dosage Form
-
Strength
12.5GM/50ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
5620
Product Number
1
Dosage Form
-
Strength
12.5GM/50ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-09-20
Active Ingredient
CEFOXITIN SODIUM
Application Number
50581
Product Number
3
Dosage Form
-
Strength
EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-09-20
Regulatory Status
Discontinued
Drug Name
MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-09-20
Active Ingredient
CEFOXITIN SODIUM
Application Number
50581
Product Number
4
Dosage Form
-
Strength
EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-09-20
Regulatory Status
Discontinued
Drug Name
MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-09-20
Active Ingredient
CEFOXITIN SODIUM
Application Number
50581
Product Number
1
Dosage Form
-
Strength
EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-09-20
Regulatory Status
Discontinued
Drug Name
MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-09-20
Active Ingredient
CEFOXITIN SODIUM
Application Number
50581
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-09-20
Regulatory Status
Discontinued
Drug Name
MEVACOR
Product Number
2
Dosage Form
-
Strength
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-03-28
Active Ingredient
LOVASTATIN
Application Number
19643
Product Number
2
Dosage Form
-
Strength
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-03-28
Regulatory Status
Discontinued
Drug Name
MEVACOR
Product Number
3
Dosage Form
-
Strength
20MG **Federal Register notice that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-08-31
Active Ingredient
LOVASTATIN
Application Number
19643
Product Number
3
Dosage Form
-
Strength
20MG **Federal Register notice that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-08-31
Regulatory Status
Discontinued
Drug Name
MEVACOR
Product Number
4
Dosage Form
-
Strength
40MG **Federal Register notice that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1988-12-14
Active Ingredient
LOVASTATIN
Application Number
19643
Product Number
4
Dosage Form
-
Strength
40MG **Federal Register notice that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1988-12-14
Regulatory Status
Discontinued
Drug Name
MODURETIC 5-50
Product Number
1
Dosage Form
-
Strength
EQ 5MG ANHYDROUS;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Application Number
18201
Product Number
1
Dosage Form
-
Strength
EQ 5MG ANHYDROUS;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
NEO-HYDELTRASOL
Product Number
1
Dosage Form
-
Strength
EQ 3.5MG BASE/GM;EQ 0.25% PHOSPHATE
Approval Date
1982-01-01
Active Ingredient
NEOMYCIN SULFATE; PREDNISOLONE SODIUM PHOSPHATE
Application Number
50378
Product Number
1
Dosage Form
-
Strength
EQ 3.5MG BASE/GM;EQ 0.25% PHOSPHATE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
NEODECADRON
Product Number
1
Dosage Form
-
Strength
EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE
Application Number
50322
Product Number
1
Dosage Form
-
Strength
EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
NEODECADRON
Product Number
1
Dosage Form
-
Strength
EQ 0.05% PHOSPHATE;EQ 3.5MG BASE/GM
Approval Date
1982-01-01
Active Ingredient
DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE
Application Number
50324
Product Number
1
Dosage Form
-
Strength
EQ 0.05% PHOSPHATE;EQ 3.5MG BASE/GM
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
NOROXIN
Product Number
2
Dosage Form
-
Strength
400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1986-10-31
Active Ingredient
NORFLOXACIN
Application Number
19384
Product Number
2
Dosage Form
-
Strength
400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1986-10-31
Regulatory Status
Discontinued
Drug Name
PEPCID
Product Number
1
Dosage Form
-
Strength
10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1986-11-04
Active Ingredient
FAMOTIDINE
Application Number
19510
Product Number
1
Dosage Form
-
Strength
10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1986-11-04
Regulatory Status
Discontinued
Drug Name
PEPCID PRESERVATIVE FREE
Product Number
4
Dosage Form
-
Strength
10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1986-11-04
Active Ingredient
FAMOTIDINE
Application Number
19510
Product Number
4
Dosage Form
-
Strength
10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1986-11-04
Regulatory Status
Discontinued
Drug Name
PEPCID RPD
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1998-05-28
Active Ingredient
FAMOTIDINE
Application Number
20752
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1998-05-28
Regulatory Status
Discontinued
Drug Name
PEPCID RPD
Product Number
2
Dosage Form
-
Strength
40MG
Approval Date
1998-05-28
Active Ingredient
FAMOTIDINE
Application Number
20752
Product Number
2
Dosage Form
-
Strength
40MG
Approval Date
1998-05-28
Regulatory Status
Discontinued
Drug Name
PERIACTIN
Product Number
1
Dosage Form
-
Strength
4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CYPROHEPTADINE HYDROCHLORIDE
Application Number
12649
Product Number
1
Dosage Form
-
Strength
4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PERIACTIN
Product Number
2
Dosage Form
-
Strength
2MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CYPROHEPTADINE HYDROCHLORIDE
Application Number
13220
Product Number
2
Dosage Form
-
Strength
2MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PRIMAXIN
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL;250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-11-26
Active Ingredient
CILASTATIN SODIUM; IMIPENEM
Application Number
50587
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL;250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-11-26
Regulatory Status
Discontinued
Drug Name
PRIMAXIN
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL;500MG/VIAL
Approval Date
1990-12-14
Active Ingredient
CILASTATIN SODIUM; IMIPENEM
Application Number
50630
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL;500MG/VIAL
Approval Date
1990-12-14
Regulatory Status
Discontinued
Drug Name
PRIMAXIN
Product Number
2
Dosage Form
-
Strength
EQ 750MG BASE/VIAL;750MG/VIAL
Approval Date
1990-12-14
Active Ingredient
CILASTATIN SODIUM; IMIPENEM
Application Number
50630
Product Number
2
Dosage Form
-
Strength
EQ 750MG BASE/VIAL;750MG/VIAL
Approval Date
1990-12-14
Regulatory Status
Discontinued
Drug Name
PRIMAXIN
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL;250MG/VIAL
Approval Date
1987-01-08
Active Ingredient
CILASTATIN SODIUM; IMIPENEM
Application Number
62756
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL;250MG/VIAL
Approval Date
1987-01-08
Regulatory Status
Discontinued
Drug Name
PRIMAXIN
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/VIAL;500MG/VIAL
Approval Date
1987-01-08
Active Ingredient
CILASTATIN SODIUM; IMIPENEM
Application Number
62756
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/VIAL;500MG/VIAL
Approval Date
1987-01-08
Regulatory Status
Discontinued
Drug Name
PRINIVIL
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1987-12-29
Active Ingredient
LISINOPRIL
Application Number
19558
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1987-12-29
Regulatory Status
Discontinued
Drug Name
PRINIVIL
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
1987-12-29
Active Ingredient
LISINOPRIL
Application Number
19558
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
1987-12-29
Regulatory Status
Discontinued
Drug Name
PRINIVIL
Product Number
3
Dosage Form
-
Strength
20MG
Approval Date
1987-12-29
Active Ingredient
LISINOPRIL
Application Number
19558
Product Number
3
Dosage Form
-
Strength
20MG
Approval Date
1987-12-29
Regulatory Status
Discontinued
Drug Name
PRINIVIL
Product Number
4
Dosage Form
-
Strength
40MG
Approval Date
1988-10-25
Active Ingredient
LISINOPRIL
Application Number
19558
Product Number
4
Dosage Form
-
Strength
40MG
Approval Date
1988-10-25
Regulatory Status
Discontinued
Drug Name
PRINIVIL
Product Number
6
Dosage Form
-
Strength
2.5MG
Approval Date
1994-01-28
Active Ingredient
LISINOPRIL
Application Number
19558
Product Number
6
Dosage Form
-
Strength
2.5MG
Approval Date
1994-01-28
Regulatory Status
Discontinued
Drug Name
PRINZIDE
Product Number
1
Dosage Form
-
Strength
12.5MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1989-02-16
Active Ingredient
HYDROCHLOROTHIAZIDE; LISINOPRIL
Application Number
19778
Product Number
1
Dosage Form
-
Strength
12.5MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1989-02-16
Regulatory Status
Discontinued
Drug Name
PRINZIDE
Product Number
2
Dosage Form
-
Strength
25MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1989-02-16
Active Ingredient
HYDROCHLOROTHIAZIDE; LISINOPRIL
Application Number
19778
Product Number
2
Dosage Form
-
Strength
25MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1989-02-16
Regulatory Status
Discontinued
Drug Name
PRINZIDE
Product Number
3
Dosage Form
-
Strength
12.5MG;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-11-18
Active Ingredient
HYDROCHLOROTHIAZIDE; LISINOPRIL
Application Number
19778
Product Number
3
Dosage Form
-
Strength
12.5MG;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-11-18
Regulatory Status
Discontinued
Drug Name
REDISOL
Product Number
10
Dosage Form
-
Strength
1MG/ML
Approval Date
1982-01-01
Active Ingredient
CYANOCOBALAMIN
Application Number
6668
Product Number
10
Dosage Form
-
Strength
1MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TIAMATE
Product Number
1
Dosage Form
-
Strength
EQ 120MG HYDROCHLORIDE
Approval Date
1996-10-04
Active Ingredient
DILTIAZEM MALATE
Application Number
20506
Product Number
1
Dosage Form
-
Strength
EQ 120MG HYDROCHLORIDE
Approval Date
1996-10-04
Regulatory Status
Discontinued
Drug Name
TIAMATE
Product Number
2
Dosage Form
-
Strength
EQ 180MG HYDROCHLORIDE
Approval Date
1996-10-04
Active Ingredient
DILTIAZEM MALATE
Application Number
20506
Product Number
2
Dosage Form
-
Strength
EQ 180MG HYDROCHLORIDE
Approval Date
1996-10-04
Regulatory Status
Discontinued
Drug Name
TIAMATE
Product Number
3
Dosage Form
-
Strength
EQ 240MG HYDROCHLORIDE
Approval Date
1996-10-04
Active Ingredient
DILTIAZEM MALATE
Application Number
20506
Product Number
3
Dosage Form
-
Strength
EQ 240MG HYDROCHLORIDE
Approval Date
1996-10-04
Regulatory Status
Discontinued
Drug Name
TIMOLIDE 10-25
Product Number
1
Dosage Form
-
Strength
25MG;10MG
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE; TIMOLOL MALEATE
Application Number
18061
Product Number
1
Dosage Form
-
Strength
25MG;10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
VIOXX
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
1999-05-20
Active Ingredient
ROFECOXIB
Application Number
21042
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
1999-05-20
Regulatory Status
Discontinued
Drug Name
VIOXX
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1999-05-20
Active Ingredient
ROFECOXIB
Application Number
21042
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1999-05-20
Regulatory Status
Discontinued
Drug Name
VIOXX
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
2000-02-25
Active Ingredient
ROFECOXIB
Application Number
21042
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
2000-02-25
Regulatory Status
Discontinued
Drug Name
VIOXX
Product Number
1
Dosage Form
-
Strength
12.5MG/5ML
Approval Date
1999-05-20
Active Ingredient
ROFECOXIB
Application Number
21052
Product Number
1
Dosage Form
-
Strength
12.5MG/5ML
Approval Date
1999-05-20
Regulatory Status
Discontinued
Drug Name
VIOXX
Product Number
2
Dosage Form
-
Strength
25MG/5ML
Approval Date
1999-05-20
Active Ingredient
ROFECOXIB
Application Number
21052
Product Number
2
Dosage Form
-
Strength
25MG/5ML
Approval Date
1999-05-20
Regulatory Status
Discontinued
Drug Status Breakdown
125 total- Discontinued
Official Source
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Drug Name
AFRINOL
Application Number
18191
Product Number
1
Active Ingredient
PSEUDOEPHEDRINE SULFATE
Dosage Form
-
Strength
120MG
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