ANI Pharmaceuticals Inc Discontinued
FDA Approved Drugs
ANI Pharmaceuticals Inc 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 331
- Latest Approval Date Jan 25, 2024
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Company
ANI Pharmaceuticals Inc Discontinued
Country
U.S.A
Website
Social Profiles
Company Snapshot
ANI Pharmaceuticals Inc Discontinued
210 Main Street West Baudette, MN 56623
U.S.A
www.anipharmaceuticals.com/ rob.schrepfer@anipharmaceuticals.com View on MapFDA Approved Drug Records ( 331 records )
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
1985-03-06
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Application Number
88629
Product Number
1
Dosage Form
-
Strength
300MG;60MG
Approval Date
1985-03-06
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
2
Dosage Form
-
Strength
300MG;15MG
Approval Date
1985-03-06
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Application Number
88629
Product Number
2
Dosage Form
-
Strength
300MG;15MG
Approval Date
1985-03-06
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
3
Dosage Form
-
Strength
300MG;30MG
Approval Date
1985-03-06
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Application Number
88629
Product Number
3
Dosage Form
-
Strength
300MG;30MG
Approval Date
1985-03-06
Regulatory Status
Discontinued
Drug Name
ACETOHEXAMIDE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1987-02-09
Active Ingredient
ACETOHEXAMIDE
Application Number
70870
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1987-02-09
Regulatory Status
Discontinued
Drug Name
ACETOHEXAMIDE
Product Number
2
Dosage Form
-
Strength
250MG
Approval Date
1987-02-09
Active Ingredient
ACETOHEXAMIDE
Application Number
70870
Product Number
2
Dosage Form
-
Strength
250MG
Approval Date
1987-02-09
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
1
Dosage Form
-
Strength
0.25MG
Approval Date
1994-02-16
Active Ingredient
ALPRAZOLAM
Application Number
74085
Product Number
1
Dosage Form
-
Strength
0.25MG
Approval Date
1994-02-16
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
2
Dosage Form
-
Strength
0.5MG
Approval Date
1994-02-16
Active Ingredient
ALPRAZOLAM
Application Number
74085
Product Number
2
Dosage Form
-
Strength
0.5MG
Approval Date
1994-02-16
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
3
Dosage Form
-
Strength
1MG
Approval Date
1994-02-16
Active Ingredient
ALPRAZOLAM
Application Number
74085
Product Number
3
Dosage Form
-
Strength
1MG
Approval Date
1994-02-16
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
4
Dosage Form
-
Strength
2MG
Approval Date
1996-02-26
Active Ingredient
ALPRAZOLAM
Application Number
74085
Product Number
4
Dosage Form
-
Strength
2MG
Approval Date
1996-02-26
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
1
Dosage Form
-
Strength
0.5MG
Approval Date
2006-07-31
Active Ingredient
ALPRAZOLAM
Application Number
77725
Product Number
1
Dosage Form
-
Strength
0.5MG
Approval Date
2006-07-31
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
2
Dosage Form
-
Strength
1MG
Approval Date
2006-07-31
Active Ingredient
ALPRAZOLAM
Application Number
77725
Product Number
2
Dosage Form
-
Strength
1MG
Approval Date
2006-07-31
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
3
Dosage Form
-
Strength
3MG
Approval Date
2006-07-31
Active Ingredient
ALPRAZOLAM
Application Number
77725
Product Number
3
Dosage Form
-
Strength
3MG
Approval Date
2006-07-31
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
4
Dosage Form
-
Strength
2MG
Approval Date
2006-07-31
Active Ingredient
ALPRAZOLAM
Application Number
77725
Product Number
4
Dosage Form
-
Strength
2MG
Approval Date
2006-07-31
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
1
Dosage Form
-
Strength
0.5MG
Approval Date
2007-02-28
Active Ingredient
ALPRAZOLAM
Application Number
77979
Product Number
1
Dosage Form
-
Strength
0.5MG
Approval Date
2007-02-28
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
2
Dosage Form
-
Strength
1MG
Approval Date
2007-02-28
Active Ingredient
ALPRAZOLAM
Application Number
77979
Product Number
2
Dosage Form
-
Strength
1MG
Approval Date
2007-02-28
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
3
Dosage Form
-
Strength
2MG
Approval Date
2007-02-28
Active Ingredient
ALPRAZOLAM
Application Number
77979
Product Number
3
Dosage Form
-
Strength
2MG
Approval Date
2007-02-28
Regulatory Status
Discontinued
Drug Name
ALPRAZOLAM
Product Number
4
Dosage Form
-
Strength
3MG
Approval Date
2007-02-28
Active Ingredient
ALPRAZOLAM
Application Number
77979
Product Number
4
Dosage Form
-
Strength
3MG
Approval Date
2007-02-28
Regulatory Status
Discontinued
Drug Name
AMINOCAPROIC ACID
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
2020-12-14
Active Ingredient
AMINOCAPROIC ACID
Application Number
211629
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
2020-12-14
Regulatory Status
Discontinued
Drug Name
AMINOPHYLLINE
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Active Ingredient
AMINOPHYLLINE
Application Number
85261
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
AMINOPHYLLINE
Product Number
4
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Active Ingredient
AMINOPHYLLINE
Application Number
85261
Product Number
4
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
AMITRIPTYLINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
AMITRIPTYLINE HYDROCHLORIDE
Application Number
85031
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
AMITRIPTYLINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
AMITRIPTYLINE HYDROCHLORIDE
Application Number
85031
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
AMITRIPTYLINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Active Ingredient
AMITRIPTYLINE HYDROCHLORIDE
Application Number
85031
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
AMITRIPTYLINE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
75MG
Approval Date
1982-01-01
Active Ingredient
AMITRIPTYLINE HYDROCHLORIDE
Application Number
85031
Product Number
4
Dosage Form
-
Strength
75MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ASPIRIN AND DIPYRIDAMOLE
Product Number
1
Dosage Form
-
Strength
25MG;200MG
Approval Date
2017-01-18
Active Ingredient
ASPIRIN; DIPYRIDAMOLE
Application Number
206964
Product Number
1
Dosage Form
-
Strength
25MG;200MG
Approval Date
2017-01-18
Regulatory Status
Discontinued
Drug Name
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
5MG;6.25MG
Approval Date
2004-02-11
Active Ingredient
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Application Number
76348
Product Number
1
Dosage Form
-
Strength
5MG;6.25MG
Approval Date
2004-02-11
Regulatory Status
Discontinued
Drug Name
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Product Number
2
Dosage Form
-
Strength
10MG;12.5MG
Approval Date
2004-02-11
Active Ingredient
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Application Number
76348
Product Number
2
Dosage Form
-
Strength
10MG;12.5MG
Approval Date
2004-02-11
Regulatory Status
Discontinued
Drug Name
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Product Number
3
Dosage Form
-
Strength
20MG;12.5MG
Approval Date
2004-02-11
Active Ingredient
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Application Number
76348
Product Number
3
Dosage Form
-
Strength
20MG;12.5MG
Approval Date
2004-02-11
Regulatory Status
Discontinued
Drug Name
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Product Number
4
Dosage Form
-
Strength
20MG;25MG
Approval Date
2004-02-11
Active Ingredient
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Application Number
76348
Product Number
4
Dosage Form
-
Strength
20MG;25MG
Approval Date
2004-02-11
Regulatory Status
Discontinued
Drug Name
CARBIDOPA
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2014-03-10
Active Ingredient
CARBIDOPA
Application Number
203261
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2014-03-10
Regulatory Status
Discontinued
Drug Name
CARBIDOPA AND LEVODOPA
Product Number
1
Dosage Form
-
Strength
25MG;100MG
Approval Date
1995-06-29
Active Ingredient
CARBIDOPA; LEVODOPA
Application Number
73587
Product Number
1
Dosage Form
-
Strength
25MG;100MG
Approval Date
1995-06-29
Regulatory Status
Discontinued
Drug Name
CARBIDOPA AND LEVODOPA
Product Number
2
Dosage Form
-
Strength
10MG;100MG
Approval Date
1995-06-29
Active Ingredient
CARBIDOPA; LEVODOPA
Application Number
73587
Product Number
2
Dosage Form
-
Strength
10MG;100MG
Approval Date
1995-06-29
Regulatory Status
Discontinued
Drug Name
CARBIDOPA AND LEVODOPA
Product Number
3
Dosage Form
-
Strength
25MG;250MG
Approval Date
1995-06-29
Active Ingredient
CARBIDOPA; LEVODOPA
Application Number
73587
Product Number
3
Dosage Form
-
Strength
25MG;250MG
Approval Date
1995-06-29
Regulatory Status
Discontinued
Drug Name
CARBOPROST TROMETHAMINE
Product Number
1
Dosage Form
-
Strength
EQ 0.25MG BASE/ML
Approval Date
2024-01-25
Active Ingredient
CARBOPROST TROMETHAMINE
Application Number
215901
Product Number
1
Dosage Form
-
Strength
EQ 0.25MG BASE/ML
Approval Date
2024-01-25
Regulatory Status
Discontinued
Drug Name
CEFADROXIL
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/5ML
Approval Date
1989-03-01
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
62698
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/5ML
Approval Date
1989-03-01
Regulatory Status
Discontinued
Drug Name
CEFADROXIL
Product Number
2
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
1989-03-01
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
62698
Product Number
2
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
1989-03-01
Regulatory Status
Discontinued
Drug Name
CEFADROXIL
Product Number
3
Dosage Form
-
Strength
EQ 500MG BASE/5ML
Approval Date
1989-03-01
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
62698
Product Number
3
Dosage Form
-
Strength
EQ 500MG BASE/5ML
Approval Date
1989-03-01
Regulatory Status
Discontinued
Drug Name
CEFADROXIL
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
2006-01-20
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
65278
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
2006-01-20
Regulatory Status
Discontinued
Drug Name
CEFADROXIL
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/5ML
Approval Date
2006-01-20
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
65278
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/5ML
Approval Date
2006-01-20
Regulatory Status
Discontinued
Drug Name
CEFUROXIME AXETIL
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
2004-10-18
Active Ingredient
CEFUROXIME AXETIL
Application Number
65190
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
2004-10-18
Regulatory Status
Discontinued
Drug Name
CEFUROXIME AXETIL
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
2004-10-18
Active Ingredient
CEFUROXIME AXETIL
Application Number
65190
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
2004-10-18
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Active Ingredient
CHLORPROPAMIDE
Application Number
87353
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1984-10-11
Active Ingredient
CHLORPROPAMIDE
Application Number
88768
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1984-10-11
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1984-10-19
Active Ingredient
CHLORPROPAMIDE
Application Number
88812
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1984-10-19
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1984-10-19
Active Ingredient
CHLORPROPAMIDE
Application Number
88813
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1984-10-19
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1984-09-26
Active Ingredient
CHLORPROPAMIDE
Application Number
88826
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1984-09-26
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1984-10-25
Active Ingredient
CHLORPROPAMIDE
Application Number
88840
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1984-10-25
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1984-10-16
Active Ingredient
CHLORPROPAMIDE
Application Number
88918
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1984-10-16
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1984-10-16
Active Ingredient
CHLORPROPAMIDE
Application Number
88919
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1984-10-16
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1985-04-12
Active Ingredient
CHLORPROPAMIDE
Application Number
88921
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1985-04-12
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1985-04-12
Active Ingredient
CHLORPROPAMIDE
Application Number
88922
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1985-04-12
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1986-11-17
Active Ingredient
CHLORPROPAMIDE
Application Number
89446
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1986-11-17
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1986-11-17
Active Ingredient
CHLORPROPAMIDE
Application Number
89447
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1986-11-17
Regulatory Status
Discontinued
Drug Name
CHLORTHALIDONE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
CHLORTHALIDONE
Application Number
87296
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORTHALIDONE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Active Ingredient
CHLORTHALIDONE
Application Number
87689
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORTHALIDONE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
CHLORTHALIDONE
Application Number
87706
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORTHALIDONE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1984-01-09
Active Ingredient
CHLORTHALIDONE
Application Number
88164
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1984-01-09
Regulatory Status
Discontinued
Drug Name
CHOLESTYRAMINE
Product Number
1
Dosage Form
-
Strength
EQ 4GM RESIN/PACKET
Approval Date
1996-10-02
Active Ingredient
CHOLESTYRAMINE
Application Number
74554
Product Number
1
Dosage Form
-
Strength
EQ 4GM RESIN/PACKET
Approval Date
1996-10-02
Regulatory Status
Discontinued
Drug Name
CHOLESTYRAMINE
Product Number
2
Dosage Form
-
Strength
EQ 4GM RESIN/SCOOPFUL
Approval Date
1996-10-02
Active Ingredient
CHOLESTYRAMINE
Application Number
74554
Product Number
2
Dosage Form
-
Strength
EQ 4GM RESIN/SCOOPFUL
Approval Date
1996-10-02
Regulatory Status
Discontinued
Drug Name
CIMETIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
1996-09-26
Active Ingredient
CIMETIDINE HYDROCHLORIDE
Application Number
74610
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
1996-09-26
Regulatory Status
Discontinued
Drug Name
CIMETIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
1998-07-09
Active Ingredient
CIMETIDINE HYDROCHLORIDE
Application Number
74859
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
1998-07-09
Regulatory Status
Discontinued
Drug Name
CIMETIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
1998-06-18
Active Ingredient
CIMETIDINE HYDROCHLORIDE
Application Number
75110
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
1998-06-18
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN EXTENDED RELEASE
Product Number
1
Dosage Form
-
Strength
425.2MG;EQ 574.9MG BASE
Approval Date
2010-11-30
Active Ingredient
CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Application Number
77809
Product Number
1
Dosage Form
-
Strength
425.2MG;EQ 574.9MG BASE
Approval Date
2010-11-30
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN EXTENDED RELEASE
Product Number
2
Dosage Form
-
Strength
212.6MG;EQ 287.5MG BASE
Approval Date
2010-11-30
Active Ingredient
CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Application Number
77809
Product Number
2
Dosage Form
-
Strength
212.6MG;EQ 287.5MG BASE
Approval Date
2010-11-30
Regulatory Status
Discontinued
Drug Name
CLARITHROMYCIN
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
2005-08-25
Active Ingredient
CLARITHROMYCIN
Application Number
65250
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
2005-08-25
Regulatory Status
Discontinued
Drug Name
CLEMASTINE FUMARATE
Product Number
1
Dosage Form
-
Strength
1.34MG
Approval Date
1992-01-31
Active Ingredient
CLEMASTINE FUMARATE
Application Number
73282
Product Number
1
Dosage Form
-
Strength
1.34MG
Approval Date
1992-01-31
Regulatory Status
Discontinued
Drug Name
CLEMASTINE FUMARATE
Product Number
2
Dosage Form
-
Strength
1.34MG
Approval Date
1992-12-03
Active Ingredient
CLEMASTINE FUMARATE
Application Number
73282
Product Number
2
Dosage Form
-
Strength
1.34MG
Approval Date
1992-12-03
Regulatory Status
Discontinued
Drug Name
CLOBETASOL PROPIONATE (EMOLLIENT)
Product Number
1
Dosage Form
-
Strength
0.05%
Approval Date
2001-08-22
Active Ingredient
CLOBETASOL PROPIONATE
Application Number
75733
Product Number
1
Dosage Form
-
Strength
0.05%
Approval Date
2001-08-22
Regulatory Status
Discontinued
Drug Name
CLOPIDOGREL BISULFATE
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
2012-05-17
Active Ingredient
CLOPIDOGREL BISULFATE
Application Number
90625
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
2012-05-17
Regulatory Status
Discontinued
Drug Name
CLOPIDOGREL BISULFATE
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
2012-05-17
Active Ingredient
CLOPIDOGREL BISULFATE
Application Number
91216
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
2012-05-17
Regulatory Status
Discontinued
Drug Name
CORTROPHIN-ZINC
Product Number
1
Dosage Form
-
Strength
40 UNITS/ML
Approval Date
1982-01-01
Active Ingredient
CORTICOTROPIN-ZINC HYDROXIDE
Application Number
9854
Product Number
1
Dosage Form
-
Strength
40 UNITS/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CYCLOPHOSPHAMIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2018-03-19
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
207014
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2018-03-19
Regulatory Status
Discontinued
Drug Name
CYCLOPHOSPHAMIDE
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2018-03-19
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
207014
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2018-03-19
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1997-05-29
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
71803
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1997-05-29
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1987-12-08
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
71803
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1987-12-08
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
1987-12-08
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
71803
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
1987-12-08
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
75MG
Approval Date
1987-12-08
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
71803
Product Number
4
Dosage Form
-
Strength
75MG
Approval Date
1987-12-08
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
5
Dosage Form
-
Strength
150MG
Approval Date
1997-05-29
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
71803
Product Number
5
Dosage Form
-
Strength
150MG
Approval Date
1997-05-29
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2016-10-28
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
205153
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2016-10-28
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
2016-10-28
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
205153
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
2016-10-28
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
2016-10-28
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
205153
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
2016-10-28
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
75MG
Approval Date
2016-10-28
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
205153
Product Number
4
Dosage Form
-
Strength
75MG
Approval Date
2016-10-28
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
5
Dosage Form
-
Strength
100MG
Approval Date
2016-10-28
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
205153
Product Number
5
Dosage Form
-
Strength
100MG
Approval Date
2016-10-28
Regulatory Status
Discontinued
Drug Name
DESIPRAMINE HYDROCHLORIDE
Product Number
6
Dosage Form
-
Strength
150MG
Approval Date
2016-10-28
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
205153
Product Number
6
Dosage Form
-
Strength
150MG
Approval Date
2016-10-28
Regulatory Status
Discontinued
Drug Name
DEXCHLORPHENIRAMINE MALEATE
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
1986-01-17
Active Ingredient
DEXCHLORPHENIRAMINE MALEATE
Application Number
88682
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
1986-01-17
Regulatory Status
Discontinued
Drug Name
DEXTROAMPHETAMINE SULFATE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Active Ingredient
DEXTROAMPHETAMINE SULFATE
Application Number
85370
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DIFLORASONE DIACETATE
Product Number
1
Dosage Form
-
Strength
0.05%
Approval Date
2002-12-20
Active Ingredient
DIFLORASONE DIACETATE
Application Number
76263
Product Number
1
Dosage Form
-
Strength
0.05%
Approval Date
2002-12-20
Regulatory Status
Discontinued
Drug Name
DIFLUNISAL
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1996-06-10
Active Ingredient
DIFLUNISAL
Application Number
74604
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1996-06-10
Regulatory Status
Discontinued
Drug Name
DIPYRIDAMOLE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1992-02-25
Active Ingredient
DIPYRIDAMOLE
Application Number
86944
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1992-02-25
Regulatory Status
Discontinued
Drug Name
DIPYRIDAMOLE
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1991-04-16
Active Ingredient
DIPYRIDAMOLE
Application Number
86944
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1991-04-16
Regulatory Status
Discontinued
Drug Name
DIPYRIDAMOLE
Product Number
3
Dosage Form
-
Strength
75MG
Approval Date
1992-02-25
Active Ingredient
DIPYRIDAMOLE
Application Number
86944
Product Number
3
Dosage Form
-
Strength
75MG
Approval Date
1992-02-25
Regulatory Status
Discontinued
Drug Name
DOXAZOSIN MESYLATE
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
2000-10-18
Active Ingredient
DOXAZOSIN MESYLATE
Application Number
75432
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
2000-10-18
Regulatory Status
Discontinued
Drug Name
DOXAZOSIN MESYLATE
Product Number
2
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2000-10-18
Active Ingredient
DOXAZOSIN MESYLATE
Application Number
75432
Product Number
2
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2000-10-18
Regulatory Status
Discontinued
Drug Name
DOXAZOSIN MESYLATE
Product Number
3
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2000-10-18
Active Ingredient
DOXAZOSIN MESYLATE
Application Number
75432
Product Number
3
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2000-10-18
Regulatory Status
Discontinued
Drug Name
DOXAZOSIN MESYLATE
Product Number
4
Dosage Form
-
Strength
EQ 8MG BASE
Approval Date
2000-10-18
Active Ingredient
DOXAZOSIN MESYLATE
Application Number
75432
Product Number
4
Dosage Form
-
Strength
EQ 8MG BASE
Approval Date
2000-10-18
Regulatory Status
Discontinued
Drug Name
ERYTHROMYCIN STEARATE
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Active Ingredient
ERYTHROMYCIN STEARATE
Application Number
61461
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ERYTHROMYCIN STEARATE
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1982-01-01
Active Ingredient
ERYTHROMYCIN STEARATE
Application Number
61461
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ERYTHROMYCIN STEARATE
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Active Ingredient
ERYTHROMYCIN STEARATE
Application Number
61591
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ERYTHROMYCIN STEARATE
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1990-05-15
Active Ingredient
ERYTHROMYCIN STEARATE
Application Number
63179
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1990-05-15
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1997-08-29
Active Ingredient
ETODOLAC
Application Number
74840
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1997-08-29
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
1997-08-29
Active Ingredient
ETODOLAC
Application Number
74840
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
1997-08-29
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1997-12-23
Active Ingredient
ETODOLAC
Application Number
74844
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1997-12-23
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
1997-12-23
Active Ingredient
ETODOLAC
Application Number
74844
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
1997-12-23
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1997-07-08
Active Ingredient
ETODOLAC
Application Number
74899
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1997-07-08
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
1997-07-08
Active Ingredient
ETODOLAC
Application Number
74899
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
1997-07-08
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
2002-07-26
Active Ingredient
ETODOLAC
Application Number
75943
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
2002-07-26
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
2002-07-26
Active Ingredient
ETODOLAC
Application Number
75943
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
2002-07-26
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
3
Dosage Form
-
Strength
600MG
Approval Date
2002-07-26
Active Ingredient
ETODOLAC
Application Number
75943
Product Number
3
Dosage Form
-
Strength
600MG
Approval Date
2002-07-26
Regulatory Status
Discontinued
Drug Name
EXTENDED PHENYTOIN SODIUM
Product Number
1
Dosage Form
-
Strength
100MG EXTENDED
Approval Date
2003-06-20
Active Ingredient
PHENYTOIN SODIUM
Application Number
40435
Product Number
1
Dosage Form
-
Strength
100MG EXTENDED
Approval Date
2003-06-20
Regulatory Status
Discontinued
Drug Name
EXTENDED PHENYTOIN SODIUM
Product Number
1
Dosage Form
-
Strength
100MG EXTENDED
Approval Date
1986-12-18
Active Ingredient
PHENYTOIN SODIUM
Application Number
89441
Product Number
1
Dosage Form
-
Strength
100MG EXTENDED
Approval Date
1986-12-18
Regulatory Status
Discontinued
Drug Name
EZETIMIBE AND SIMVASTATIN
Product Number
1
Dosage Form
-
Strength
10MG;10MG
Approval Date
2017-04-26
Active Ingredient
EZETIMIBE; SIMVASTATIN
Application Number
201890
Product Number
1
Dosage Form
-
Strength
10MG;10MG
Approval Date
2017-04-26
Regulatory Status
Discontinued
Drug Name
EZETIMIBE AND SIMVASTATIN
Product Number
2
Dosage Form
-
Strength
10MG;20MG
Approval Date
2017-04-26
Active Ingredient
EZETIMIBE; SIMVASTATIN
Application Number
201890
Product Number
2
Dosage Form
-
Strength
10MG;20MG
Approval Date
2017-04-26
Regulatory Status
Discontinued
Drug Name
EZETIMIBE AND SIMVASTATIN
Product Number
3
Dosage Form
-
Strength
10MG;40MG
Approval Date
2017-04-26
Active Ingredient
EZETIMIBE; SIMVASTATIN
Application Number
201890
Product Number
3
Dosage Form
-
Strength
10MG;40MG
Approval Date
2017-04-26
Regulatory Status
Discontinued
Drug Name
EZETIMIBE AND SIMVASTATIN
Product Number
4
Dosage Form
-
Strength
10MG;80MG
Approval Date
2017-04-26
Active Ingredient
EZETIMIBE; SIMVASTATIN
Application Number
201890
Product Number
4
Dosage Form
-
Strength
10MG;80MG
Approval Date
2017-04-26
Regulatory Status
Discontinued
Drug Name
FENOPROFEN CALCIUM
Product Number
1
Dosage Form
-
Strength
EQ 600MG BASE
Approval Date
1988-05-02
Active Ingredient
FENOPROFEN CALCIUM
Application Number
72274
Product Number
1
Dosage Form
-
Strength
EQ 600MG BASE
Approval Date
1988-05-02
Regulatory Status
Discontinued
Drug Name
FESOTERODINE FUMARATE
Product Number
1
Dosage Form
-
Strength
4MG
Approval Date
2023-01-04
Active Ingredient
FESOTERODINE FUMARATE
Application Number
204504
Product Number
1
Dosage Form
-
Strength
4MG
Approval Date
2023-01-04
Regulatory Status
Discontinued
Drug Name
FESOTERODINE FUMARATE
Product Number
2
Dosage Form
-
Strength
8MG
Approval Date
2023-01-04
Active Ingredient
FESOTERODINE FUMARATE
Application Number
204504
Product Number
2
Dosage Form
-
Strength
8MG
Approval Date
2023-01-04
Regulatory Status
Discontinued
Drug Name
FLECAINIDE ACETATE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
2002-10-28
Active Ingredient
FLECAINIDE ACETATE
Application Number
76030
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
2002-10-28
Regulatory Status
Discontinued
Drug Name
FLECAINIDE ACETATE
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
2002-10-28
Active Ingredient
FLECAINIDE ACETATE
Application Number
76030
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
2002-10-28
Regulatory Status
Discontinued
Drug Name
FLECAINIDE ACETATE
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
2002-10-28
Active Ingredient
FLECAINIDE ACETATE
Application Number
76030
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
2002-10-28
Regulatory Status
Discontinued
Drug Name
FLUCONAZOLE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
2004-07-29
Active Ingredient
FLUCONAZOLE
Application Number
76086
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
2004-07-29
Regulatory Status
Discontinued
Drug Name
FLUCONAZOLE
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
2004-07-29
Active Ingredient
FLUCONAZOLE
Application Number
76086
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
2004-07-29
Regulatory Status
Discontinued
Drug Name
FLUCONAZOLE
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
2004-07-29
Active Ingredient
FLUCONAZOLE
Application Number
76086
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
2004-07-29
Regulatory Status
Discontinued
Drug Name
FLUCONAZOLE
Product Number
4
Dosage Form
-
Strength
200MG
Approval Date
2004-07-29
Active Ingredient
FLUCONAZOLE
Application Number
76086
Product Number
4
Dosage Form
-
Strength
200MG
Approval Date
2004-07-29
Regulatory Status
Discontinued
Drug Name
FLUOXETINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
2008-05-20
Active Ingredient
FLUOXETINE HYDROCHLORIDE
Application Number
76287
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
2008-05-20
Regulatory Status
Discontinued
Drug Name
FLUOXETINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE
Approval Date
2008-05-20
Active Ingredient
FLUOXETINE HYDROCHLORIDE
Application Number
76287
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE
Approval Date
2008-05-20
Regulatory Status
Discontinued
Drug Name
FLUPHENAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG/ML
Approval Date
1991-08-30
Active Ingredient
FLUPHENAZINE HYDROCHLORIDE
Application Number
73058
Product Number
1
Dosage Form
-
Strength
5MG/ML
Approval Date
1991-08-30
Regulatory Status
Discontinued
Drug Name
FLUPHENAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
2.5MG/5ML
Approval Date
1993-04-29
Active Ingredient
FLUPHENAZINE HYDROCHLORIDE
Application Number
81310
Product Number
1
Dosage Form
-
Strength
2.5MG/5ML
Approval Date
1993-04-29
Regulatory Status
Discontinued
Drug Name
FLUVOXAMINE MALEATE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2001-01-25
Active Ingredient
FLUVOXAMINE MALEATE
Application Number
75897
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2001-01-25
Regulatory Status
Discontinued
Drug Name
FLUVOXAMINE MALEATE
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2001-01-25
Active Ingredient
FLUVOXAMINE MALEATE
Application Number
75897
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2001-01-25
Regulatory Status
Discontinued
Drug Name
FLUVOXAMINE MALEATE
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2001-01-25
Active Ingredient
FLUVOXAMINE MALEATE
Application Number
75897
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2001-01-25
Regulatory Status
Discontinued
Drug Name
FLUVOXAMINE MALEATE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2001-03-12
Active Ingredient
FLUVOXAMINE MALEATE
Application Number
75898
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2001-03-12
Regulatory Status
Discontinued
Drug Name
FLUVOXAMINE MALEATE
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2001-03-12
Active Ingredient
FLUVOXAMINE MALEATE
Application Number
75898
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2001-03-12
Regulatory Status
Discontinued
Drug Name
FLUVOXAMINE MALEATE
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2001-03-12
Active Ingredient
FLUVOXAMINE MALEATE
Application Number
75898
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2001-03-12
Regulatory Status
Discontinued
Drug Name
FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
10MG;12.5MG
Approval Date
2004-12-03
Active Ingredient
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Application Number
76608
Product Number
1
Dosage Form
-
Strength
10MG;12.5MG
Approval Date
2004-12-03
Regulatory Status
Discontinued
Drug Name
FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
Product Number
2
Dosage Form
-
Strength
20MG;12.5MG
Approval Date
2004-12-03
Active Ingredient
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Application Number
76608
Product Number
2
Dosage Form
-
Strength
20MG;12.5MG
Approval Date
2004-12-03
Regulatory Status
Discontinued
Drug Name
FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
10MG;12.5MG
Approval Date
2005-08-16
Active Ingredient
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Application Number
77144
Product Number
1
Dosage Form
-
Strength
10MG;12.5MG
Approval Date
2005-08-16
Regulatory Status
Discontinued
Drug Name
FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
Product Number
2
Dosage Form
-
Strength
20MG;12.5MG
Approval Date
2005-08-16
Active Ingredient
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Application Number
77144
Product Number
2
Dosage Form
-
Strength
20MG;12.5MG
Approval Date
2005-08-16
Regulatory Status
Discontinued
Drug Name
FUROSEMIDE
Product Number
1
Dosage Form
-
Strength
40MG
Approval Date
1986-02-26
Active Ingredient
FUROSEMIDE
Application Number
70413
Product Number
1
Dosage Form
-
Strength
40MG
Approval Date
1986-02-26
Regulatory Status
Discontinued
Drug Name
FUROSEMIDE
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1987-01-02
Active Ingredient
FUROSEMIDE
Application Number
71379
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1987-01-02
Regulatory Status
Discontinued
Drug Name
FUROSEMIDE
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
1988-02-09
Active Ingredient
FUROSEMIDE
Application Number
71594
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
1988-02-09
Regulatory Status
Discontinued
Drug Name
GLIPIZIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1996-03-04
Active Ingredient
GLIPIZIDE
Application Number
74387
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1996-03-04
Regulatory Status
Discontinued
Drug Name
GLIPIZIDE
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
1996-03-04
Active Ingredient
GLIPIZIDE
Application Number
74387
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
1996-03-04
Regulatory Status
Discontinued
Drug Name
GLUCAMIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1984-10-11
Active Ingredient
CHLORPROPAMIDE
Application Number
88641
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1984-10-11
Regulatory Status
Discontinued
Drug Name
GUANABENZ ACETATE
Product Number
1
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
1995-04-07
Active Ingredient
GUANABENZ ACETATE
Application Number
74149
Product Number
1
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
1995-04-07
Regulatory Status
Discontinued
Drug Name
GUANABENZ ACETATE
Product Number
2
Dosage Form
-
Strength
EQ 8MG BASE
Approval Date
1995-04-07
Active Ingredient
GUANABENZ ACETATE
Application Number
74149
Product Number
2
Dosage Form
-
Strength
EQ 8MG BASE
Approval Date
1995-04-07
Regulatory Status
Discontinued
Drug Name
GUANABENZ ACETATE
Product Number
1
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
1994-06-01
Active Ingredient
GUANABENZ ACETATE
Application Number
74267
Product Number
1
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
1994-06-01
Regulatory Status
Discontinued
Drug Name
GUANABENZ ACETATE
Product Number
2
Dosage Form
-
Strength
EQ 8MG BASE
Approval Date
1994-06-01
Active Ingredient
GUANABENZ ACETATE
Application Number
74267
Product Number
2
Dosage Form
-
Strength
EQ 8MG BASE
Approval Date
1994-06-01
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND IBUPROFEN
Product Number
1
Dosage Form
-
Strength
5MG;200MG
Approval Date
2010-06-23
Active Ingredient
HYDROCODONE BITARTRATE; IBUPROFEN
Application Number
77454
Product Number
1
Dosage Form
-
Strength
5MG;200MG
Approval Date
2010-06-23
Regulatory Status
Discontinued
Drug Name
IBUPROFEN
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1987-01-20
Active Ingredient
IBUPROFEN
Application Number
71144
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1987-01-20
Regulatory Status
Discontinued
Drug Name
IBUPROFEN
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1991-12-19
Active Ingredient
IBUPROFEN
Application Number
72901
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1991-12-19
Regulatory Status
Discontinued
Drug Name
IBUPROFEN
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1991-12-19
Active Ingredient
IBUPROFEN
Application Number
72903
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1991-12-19
Regulatory Status
Discontinued
Drug Name
INDAPAMIDE
Product Number
1
Dosage Form
-
Strength
2.5MG
Approval Date
1996-10-31
Active Ingredient
INDAPAMIDE
Application Number
74498
Product Number
1
Dosage Form
-
Strength
2.5MG
Approval Date
1996-10-31
Regulatory Status
Discontinued
Drug Name
INDAPAMIDE
Product Number
2
Dosage Form
-
Strength
1.25MG
Approval Date
1998-02-12
Active Ingredient
INDAPAMIDE
Application Number
74498
Product Number
2
Dosage Form
-
Strength
1.25MG
Approval Date
1998-02-12
Regulatory Status
Discontinued
Drug Name
INDAPAMIDE
Product Number
1
Dosage Form
-
Strength
1.25MG
Approval Date
1998-12-04
Active Ingredient
INDAPAMIDE
Application Number
75201
Product Number
1
Dosage Form
-
Strength
1.25MG
Approval Date
1998-12-04
Regulatory Status
Discontinued
Drug Name
INDAPAMIDE
Product Number
2
Dosage Form
-
Strength
2.5MG
Approval Date
1998-12-04
Active Ingredient
INDAPAMIDE
Application Number
75201
Product Number
2
Dosage Form
-
Strength
2.5MG
Approval Date
1998-12-04
Regulatory Status
Discontinued
Drug Name
INDOMETHACIN
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1987-03-18
Active Ingredient
INDOMETHACIN
Application Number
71148
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1987-03-18
Regulatory Status
Discontinued
Drug Name
INDOMETHACIN
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1987-03-18
Active Ingredient
INDOMETHACIN
Application Number
71149
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1987-03-18
Regulatory Status
Discontinued
Drug Name
ISOSORBIDE DINITRATE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1988-01-07
Active Ingredient
ISOSORBIDE DINITRATE
Application Number
86032
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1988-01-07
Regulatory Status
Discontinued
Drug Name
LACTULOSE
Product Number
1
Dosage Form
-
Strength
10GM/15ML
Approval Date
2007-11-28
Active Ingredient
LACTULOSE
Application Number
78430
Product Number
1
Dosage Form
-
Strength
10GM/15ML
Approval Date
2007-11-28
Regulatory Status
Discontinued
Drug Name
LACTULOSE
Product Number
1
Dosage Form
-
Strength
10GM/15ML
Approval Date
2008-11-21
Active Ingredient
LACTULOSE
Application Number
90426
Product Number
1
Dosage Form
-
Strength
10GM/15ML
Approval Date
2008-11-21
Regulatory Status
Discontinued
Drug Name
LANSOPRAZOLE
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
2010-10-15
Active Ingredient
LANSOPRAZOLE
Application Number
78730
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
2010-10-15
Regulatory Status
Discontinued
Drug Name
LANSOPRAZOLE
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
2010-10-15
Active Ingredient
LANSOPRAZOLE
Application Number
78730
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
2010-10-15
Regulatory Status
Discontinued
Drug Name
LANSOPRAZOLE, AMOXICILLIN AND CLARITHROMYCIN (COPACKAGED)
Product Number
1
Dosage Form
-
Strength
500MG;500MG;30MG
Approval Date
2013-08-30
Active Ingredient
AMOXICILLIN; CLARITHROMYCIN; LANSOPRAZOLE
Application Number
200218
Product Number
1
Dosage Form
-
Strength
500MG;500MG;30MG
Approval Date
2013-08-30
Regulatory Status
Discontinued
Drug Name
LEUCOVORIN CALCIUM
Product Number
1
Dosage Form
-
Strength
EQ 15MG BASE
Approval Date
1999-03-24
Active Ingredient
LEUCOVORIN CALCIUM
Application Number
75327
Product Number
1
Dosage Form
-
Strength
EQ 15MG BASE
Approval Date
1999-03-24
Regulatory Status
Discontinued
Drug Name
LEVOTHYROXINE SODIUM
Product Number
1
Dosage Form
-
Strength
0.075MG
Approval Date
2020-10-28
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
211369
Product Number
1
Dosage Form
-
Strength
0.075MG
Approval Date
2020-10-28
Regulatory Status
Discontinued
Drug Name
LEVOTHYROXINE SODIUM
Product Number
2
Dosage Form
-
Strength
0.15MG
Approval Date
2020-10-28
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
211369
Product Number
2
Dosage Form
-
Strength
0.15MG
Approval Date
2020-10-28
Regulatory Status
Discontinued
Drug Name
LEVOTHYROXINE SODIUM
Product Number
3
Dosage Form
-
Strength
0.112MG
Approval Date
2021-04-16
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
211369
Product Number
3
Dosage Form
-
Strength
0.112MG
Approval Date
2021-04-16
Regulatory Status
Discontinued
Drug Name
LEVOTHYROXINE SODIUM
Product Number
4
Dosage Form
-
Strength
0.2MG
Approval Date
2022-11-09
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
211369
Product Number
4
Dosage Form
-
Strength
0.2MG
Approval Date
2022-11-09
Regulatory Status
Discontinued
Drug Name
LEVOTHYROXINE SODIUM
Product Number
5
Dosage Form
-
Strength
0.137MG
Approval Date
2023-05-02
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
211369
Product Number
5
Dosage Form
-
Strength
0.137MG
Approval Date
2023-05-02
Regulatory Status
Discontinued
Drug Name
LEVOTHYROXINE SODIUM
Product Number
6
Dosage Form
-
Strength
0.175MG
Approval Date
2023-05-02
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
211369
Product Number
6
Dosage Form
-
Strength
0.175MG
Approval Date
2023-05-02
Regulatory Status
Discontinued
Drug Name
LEVOTHYROXINE SODIUM
Product Number
1
Dosage Form
-
Strength
0.088MG
Approval Date
2021-01-06
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
213256
Product Number
1
Dosage Form
-
Strength
0.088MG
Approval Date
2021-01-06
Regulatory Status
Discontinued
Drug Name
LEVOTHYROXINE SODIUM
Product Number
2
Dosage Form
-
Strength
0.1MG
Approval Date
2021-01-06
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
213256
Product Number
2
Dosage Form
-
Strength
0.1MG
Approval Date
2021-01-06
Regulatory Status
Discontinued
Drug Name
LEVOTHYROXINE SODIUM
Product Number
3
Dosage Form
-
Strength
0.125MG
Approval Date
2021-01-06
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
213256
Product Number
3
Dosage Form
-
Strength
0.125MG
Approval Date
2021-01-06
Regulatory Status
Discontinued
Drug Name
LUXZYLA
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
2019-05-07
Active Ingredient
PENICILLAMINE
Application Number
209921
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
2019-05-07
Regulatory Status
Discontinued
Drug Name
MECLIZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
MECLIZINE HYDROCHLORIDE
Application Number
84657
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MECLIZINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
12.5MG
Approval Date
1982-01-01
Active Ingredient
MECLIZINE HYDROCHLORIDE
Application Number
84657
Product Number
2
Dosage Form
-
Strength
12.5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MECLIZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
1982-01-01
Active Ingredient
MECLIZINE HYDROCHLORIDE
Application Number
85269
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MECLIZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
MECLIZINE HYDROCHLORIDE
Application Number
85740
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MECLIZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
1985-12-11
Active Ingredient
MECLIZINE HYDROCHLORIDE
Application Number
88732
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
1985-12-11
Regulatory Status
Discontinued
Drug Name
MECLOFENAMATE SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1987-04-15
Active Ingredient
MECLOFENAMATE SODIUM
Application Number
71469
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1987-04-15
Regulatory Status
Discontinued
Drug Name
MECLOFENAMATE SODIUM
Product Number
2
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
1987-04-15
Active Ingredient
MECLOFENAMATE SODIUM
Application Number
71469
Product Number
2
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
1987-04-15
Regulatory Status
Discontinued
Drug Name
MEMANTINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
7MG
Approval Date
2020-02-28
Active Ingredient
MEMANTINE HYDROCHLORIDE
Application Number
205365
Product Number
1
Dosage Form
-
Strength
7MG
Approval Date
2020-02-28
Regulatory Status
Discontinued
Drug Name
MEMANTINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
14MG
Approval Date
2020-02-28
Active Ingredient
MEMANTINE HYDROCHLORIDE
Application Number
205365
Product Number
2
Dosage Form
-
Strength
14MG
Approval Date
2020-02-28
Regulatory Status
Discontinued
Drug Name
MEMANTINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
21MG
Approval Date
2020-02-28
Active Ingredient
MEMANTINE HYDROCHLORIDE
Application Number
205365
Product Number
3
Dosage Form
-
Strength
21MG
Approval Date
2020-02-28
Regulatory Status
Discontinued
Drug Name
MEMANTINE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
28MG
Approval Date
2020-02-28
Active Ingredient
MEMANTINE HYDROCHLORIDE
Application Number
205365
Product Number
4
Dosage Form
-
Strength
28MG
Approval Date
2020-02-28
Regulatory Status
Discontinued
Drug Name
METHOCARBAMOL
Product Number
2
Dosage Form
-
Strength
750MG
Approval Date
1982-01-01
Active Ingredient
METHOCARBAMOL
Application Number
84276
Product Number
2
Dosage Form
-
Strength
750MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
METHOCARBAMOL
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
METHOCARBAMOL
Application Number
84277
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
METHOXSALEN
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-06-08
Active Ingredient
METHOXSALEN
Application Number
87781
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-06-08
Regulatory Status
Discontinued
Drug Name
METHYLPHENIDATE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
18MG
Approval Date
2017-07-14
Active Ingredient
METHYLPHENIDATE HYDROCHLORIDE
Application Number
208607
Product Number
1
Dosage Form
-
Strength
18MG
Approval Date
2017-07-14
Regulatory Status
Discontinued
Drug Name
METHYLPHENIDATE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
27MG
Approval Date
2017-07-14
Active Ingredient
METHYLPHENIDATE HYDROCHLORIDE
Application Number
208607
Product Number
2
Dosage Form
-
Strength
27MG
Approval Date
2017-07-14
Regulatory Status
Discontinued
Drug Name
METHYLPHENIDATE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
36MG
Approval Date
2017-07-14
Active Ingredient
METHYLPHENIDATE HYDROCHLORIDE
Application Number
208607
Product Number
3
Dosage Form
-
Strength
36MG
Approval Date
2017-07-14
Regulatory Status
Discontinued
Drug Name
METHYLPHENIDATE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
54MG
Approval Date
2017-07-14
Active Ingredient
METHYLPHENIDATE HYDROCHLORIDE
Application Number
208607
Product Number
4
Dosage Form
-
Strength
54MG
Approval Date
2017-07-14
Regulatory Status
Discontinued
Drug Name
METOLAZONE
Product Number
1
Dosage Form
-
Strength
2.5MG
Approval Date
2004-01-06
Active Ingredient
METOLAZONE
Application Number
75543
Product Number
1
Dosage Form
-
Strength
2.5MG
Approval Date
2004-01-06
Regulatory Status
Discontinued
Drug Name
METOLAZONE
Product Number
2
Dosage Form
-
Strength
5MG
Approval Date
2004-03-01
Active Ingredient
METOLAZONE
Application Number
75543
Product Number
2
Dosage Form
-
Strength
5MG
Approval Date
2004-03-01
Regulatory Status
Discontinued
Drug Name
METOLAZONE
Product Number
3
Dosage Form
-
Strength
10MG
Approval Date
2003-12-24
Active Ingredient
METOLAZONE
Application Number
75543
Product Number
3
Dosage Form
-
Strength
10MG
Approval Date
2003-12-24
Regulatory Status
Discontinued
Drug Name
MORPHINE SULFATE
Product Number
1
Dosage Form
-
Strength
10MG/5ML
Approval Date
2018-04-17
Active Ingredient
MORPHINE SULFATE
Application Number
205509
Product Number
1
Dosage Form
-
Strength
10MG/5ML
Approval Date
2018-04-17
Regulatory Status
Discontinued
Drug Name
MORPHINE SULFATE
Product Number
2
Dosage Form
-
Strength
20MG/5ML
Approval Date
2018-04-17
Active Ingredient
MORPHINE SULFATE
Application Number
205509
Product Number
2
Dosage Form
-
Strength
20MG/5ML
Approval Date
2018-04-17
Regulatory Status
Discontinued
Drug Name
MORPHINE SULFATE
Product Number
3
Dosage Form
-
Strength
100MG/5ML
Approval Date
2018-04-17
Active Ingredient
MORPHINE SULFATE
Application Number
205509
Product Number
3
Dosage Form
-
Strength
100MG/5ML
Approval Date
2018-04-17
Regulatory Status
Discontinued
Drug Name
NARATRIPTAN
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
2010-07-07
Active Ingredient
NARATRIPTAN HYDROCHLORIDE
Application Number
78751
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
2010-07-07
Regulatory Status
Discontinued
Drug Name
NARATRIPTAN
Product Number
2
Dosage Form
-
Strength
EQ 2.5MG BASE
Approval Date
2010-07-07
Active Ingredient
NARATRIPTAN HYDROCHLORIDE
Application Number
78751
Product Number
2
Dosage Form
-
Strength
EQ 2.5MG BASE
Approval Date
2010-07-07
Regulatory Status
Discontinued
Drug Name
NEFAZODONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
2003-09-16
Active Ingredient
NEFAZODONE HYDROCHLORIDE
Application Number
76072
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
2003-09-16
Regulatory Status
Discontinued
Drug Name
NEFAZODONE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
2003-09-16
Active Ingredient
NEFAZODONE HYDROCHLORIDE
Application Number
76072
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
2003-09-16
Regulatory Status
Discontinued
Drug Name
NEFAZODONE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
2003-09-16
Active Ingredient
NEFAZODONE HYDROCHLORIDE
Application Number
76072
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
2003-09-16
Regulatory Status
Discontinued
Drug Name
NEFAZODONE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
200MG
Approval Date
2003-09-16
Active Ingredient
NEFAZODONE HYDROCHLORIDE
Application Number
76072
Product Number
4
Dosage Form
-
Strength
200MG
Approval Date
2003-09-16
Regulatory Status
Discontinued
Drug Name
NEFAZODONE HYDROCHLORIDE
Product Number
5
Dosage Form
-
Strength
250MG
Approval Date
2003-09-16
Active Ingredient
NEFAZODONE HYDROCHLORIDE
Application Number
76072
Product Number
5
Dosage Form
-
Strength
250MG
Approval Date
2003-09-16
Regulatory Status
Discontinued
Drug Name
NICARDIPINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1996-12-10
Active Ingredient
NICARDIPINE HYDROCHLORIDE
Application Number
74439
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1996-12-10
Regulatory Status
Discontinued
Drug Name
NICARDIPINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
1996-12-10
Active Ingredient
NICARDIPINE HYDROCHLORIDE
Application Number
74439
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
1996-12-10
Regulatory Status
Discontinued
Drug Name
NICARDIPINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1996-10-28
Active Ingredient
NICARDIPINE HYDROCHLORIDE
Application Number
74540
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1996-10-28
Regulatory Status
Discontinued
Drug Name
NICARDIPINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
1996-10-28
Active Ingredient
NICARDIPINE HYDROCHLORIDE
Application Number
74540
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
1996-10-28
Regulatory Status
Discontinued
Drug Name
NIZATIDINE
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
2002-07-08
Active Ingredient
NIZATIDINE
Application Number
75461
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
2002-07-08
Regulatory Status
Discontinued
Drug Name
NIZATIDINE
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
2002-07-08
Active Ingredient
NIZATIDINE
Application Number
75461
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
2002-07-08
Regulatory Status
Discontinued
Drug Name
NIZATIDINE
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
2002-09-12
Active Ingredient
NIZATIDINE
Application Number
75668
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
2002-09-12
Regulatory Status
Discontinued
Drug Name
NIZATIDINE
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
2002-09-12
Active Ingredient
NIZATIDINE
Application Number
75668
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
2002-09-12
Regulatory Status
Discontinued
Drug Name
NORTRIPTYLINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
1992-12-31
Active Ingredient
NORTRIPTYLINE HYDROCHLORIDE
Application Number
74054
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
1992-12-31
Regulatory Status
Discontinued
Drug Name
NORTRIPTYLINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 25MG BASE
Approval Date
1992-12-31
Active Ingredient
NORTRIPTYLINE HYDROCHLORIDE
Application Number
74054
Product Number
2
Dosage Form
-
Strength
EQ 25MG BASE
Approval Date
1992-12-31
Regulatory Status
Discontinued
Drug Name
NORTRIPTYLINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
1992-12-31
Active Ingredient
NORTRIPTYLINE HYDROCHLORIDE
Application Number
74054
Product Number
3
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
1992-12-31
Regulatory Status
Discontinued
Drug Name
NORTRIPTYLINE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
1992-12-31
Active Ingredient
NORTRIPTYLINE HYDROCHLORIDE
Application Number
74054
Product Number
4
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
1992-12-31
Regulatory Status
Discontinued
Drug Name
OXACILLIN SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Active Ingredient
OXACILLIN SODIUM
Application Number
62222
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
OXACILLIN SODIUM
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1982-01-01
Active Ingredient
OXACILLIN SODIUM
Application Number
62222
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
OXISTAT
Product Number
1
Dosage Form
-
Strength
EQ 1% BASE
Approval Date
1992-09-30
Active Ingredient
OXICONAZOLE NITRATE
Application Number
20209
Product Number
1
Dosage Form
-
Strength
EQ 1% BASE
Approval Date
1992-09-30
Regulatory Status
Discontinued
Drug Name
OXYCODONE AND ASPIRIN
Product Number
1
Dosage Form
-
Strength
325MG;4.5MG;0.38MG
Approval Date
1998-02-27
Active Ingredient
ASPIRIN; OXYCODONE HYDROCHLORIDE; OXYCODONE TEREPHTHALATE
Application Number
40255
Product Number
1
Dosage Form
-
Strength
325MG;4.5MG;0.38MG
Approval Date
1998-02-27
Regulatory Status
Discontinued
Drug Name
OXYCODONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG/5ML
Approval Date
2017-08-30
Active Ingredient
OXYCODONE HYDROCHLORIDE
Application Number
203447
Product Number
1
Dosage Form
-
Strength
100MG/5ML
Approval Date
2017-08-30
Regulatory Status
Discontinued
Drug Name
PANDEL
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
1997-02-28
Active Ingredient
HYDROCORTISONE PROBUTATE
Application Number
20453
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
1997-02-28
Regulatory Status
Discontinued
Drug Name
PENTOXIFYLLINE
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1998-09-04
Active Ingredient
PENTOXIFYLLINE
Application Number
75107
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1998-09-04
Regulatory Status
Discontinued
Drug Name
PENTOXIFYLLINE
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1999-09-03
Active Ingredient
PENTOXIFYLLINE
Application Number
75199
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1999-09-03
Regulatory Status
Discontinued
Drug Name
PERINDOPRIL ERBUMINE
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
2009-11-10
Active Ingredient
PERINDOPRIL ERBUMINE
Application Number
78138
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
2009-11-10
Regulatory Status
Discontinued
Drug Name
PERINDOPRIL ERBUMINE
Product Number
2
Dosage Form
-
Strength
4MG
Approval Date
2009-11-10
Active Ingredient
PERINDOPRIL ERBUMINE
Application Number
78138
Product Number
2
Dosage Form
-
Strength
4MG
Approval Date
2009-11-10
Regulatory Status
Discontinued
Drug Name
PERINDOPRIL ERBUMINE
Product Number
3
Dosage Form
-
Strength
8MG
Approval Date
2009-11-10
Active Ingredient
PERINDOPRIL ERBUMINE
Application Number
78138
Product Number
3
Dosage Form
-
Strength
8MG
Approval Date
2009-11-10
Regulatory Status
Discontinued
Drug Name
PERPHENAZINE
Product Number
1
Dosage Form
-
Strength
8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-09-10
Active Ingredient
PERPHENAZINE
Application Number
89456
Product Number
1
Dosage Form
-
Strength
8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-09-10
Regulatory Status
Discontinued
Drug Name
PERPHENAZINE
Product Number
1
Dosage Form
-
Strength
16MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-09-10
Active Ingredient
PERPHENAZINE
Application Number
89457
Product Number
1
Dosage Form
-
Strength
16MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-09-10
Regulatory Status
Discontinued
Drug Name
PERPHENAZINE
Product Number
1
Dosage Form
-
Strength
2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-09-10
Active Ingredient
PERPHENAZINE
Application Number
89707
Product Number
1
Dosage Form
-
Strength
2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-09-10
Regulatory Status
Discontinued
Drug Name
PERPHENAZINE
Product Number
1
Dosage Form
-
Strength
4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-09-10
Active Ingredient
PERPHENAZINE
Application Number
89708
Product Number
1
Dosage Form
-
Strength
4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-09-10
Regulatory Status
Discontinued
Drug Name
PHENERGAN VC
Product Number
3
Dosage Form
-
Strength
5MG/5ML;6.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-04-02
Active Ingredient
PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE
Application Number
8604
Product Number
3
Dosage Form
-
Strength
5MG/5ML;6.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-04-02
Regulatory Status
Discontinued
Drug Name
PHENERGAN VC W/ CODEINE
Product Number
5
Dosage Form
-
Strength
10MG/5ML;5MG/5ML;6.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-04-02
Active Ingredient
CODEINE PHOSPHATE; PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE
Application Number
8306
Product Number
5
Dosage Form
-
Strength
10MG/5ML;5MG/5ML;6.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-04-02
Regulatory Status
Discontinued
Drug Name
PHENERGAN W/ CODEINE
Product Number
4
Dosage Form
-
Strength
10MG/5ML;6.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-04-02
Active Ingredient
CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE
Application Number
8306
Product Number
4
Dosage Form
-
Strength
10MG/5ML;6.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-04-02
Regulatory Status
Discontinued
Drug Name
PRAZOSIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
1989-05-16
Active Ingredient
PRAZOSIN HYDROCHLORIDE
Application Number
72577
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
1989-05-16
Regulatory Status
Discontinued
Drug Name
PRAZOSIN HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
1989-05-16
Active Ingredient
PRAZOSIN HYDROCHLORIDE
Application Number
72577
Product Number
2
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
1989-05-16
Regulatory Status
Discontinued
Drug Name
PRAZOSIN HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
EQ 5MG BASE
Approval Date
1989-05-16
Active Ingredient
PRAZOSIN HYDROCHLORIDE
Application Number
72577
Product Number
3
Dosage Form
-
Strength
EQ 5MG BASE
Approval Date
1989-05-16
Regulatory Status
Discontinued
Drug Name
PROBENECID AND COLCHICINE
Product Number
1
Dosage Form
-
Strength
0.5MG;500MG
Approval Date
1982-01-01
Active Ingredient
COLCHICINE; PROBENECID
Application Number
83734
Product Number
1
Dosage Form
-
Strength
0.5MG;500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
1GM
Approval Date
1996-12-13
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
40111
Product Number
1
Dosage Form
-
Strength
1GM
Approval Date
1996-12-13
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1985-12-02
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
88958
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1985-12-02
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1985-12-02
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
88959
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1985-12-02
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1985-07-22
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
88974
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1985-07-22
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1986-07-01
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
89219
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1986-07-01
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
375MG
Approval Date
1986-07-01
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
89219
Product Number
2
Dosage Form
-
Strength
375MG
Approval Date
1986-07-01
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
500MG
Approval Date
1986-07-01
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
89219
Product Number
3
Dosage Form
-
Strength
500MG
Approval Date
1986-07-01
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1987-08-14
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
89369
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1987-08-14
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1987-01-09
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
89369
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1987-01-09
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
750MG
Approval Date
1987-08-14
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
89369
Product Number
3
Dosage Form
-
Strength
750MG
Approval Date
1987-08-14
Regulatory Status
Discontinued
Drug Name
PROCAINAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
750MG
Approval Date
1987-03-23
Active Ingredient
PROCAINAMIDE HYDROCHLORIDE
Application Number
89438
Product Number
1
Dosage Form
-
Strength
750MG
Approval Date
1987-03-23
Regulatory Status
Discontinued
Drug Name
PROMETHAZINE HYDROCHLORIDE PLAIN
Product Number
3
Dosage Form
-
Strength
25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
PROMETHAZINE HYDROCHLORIDE
Application Number
8381
Product Number
3
Dosage Form
-
Strength
25MG/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
PROMETHAZINE HYDROCHLORIDE PLAIN
Product Number
4
Dosage Form
-
Strength
6.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-04-18
Active Ingredient
PROMETHAZINE HYDROCHLORIDE
Application Number
8381
Product Number
4
Dosage Form
-
Strength
6.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-04-18
Regulatory Status
Discontinued
Drug Name
PROMPT PHENYTOIN SODIUM
Product Number
1
Dosage Form
-
Strength
100MG PROMPT
Approval Date
1982-01-01
Active Ingredient
PHENYTOIN SODIUM
Application Number
80259
Product Number
1
Dosage Form
-
Strength
100MG PROMPT
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
60MG
Approval Date
1987-07-15
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
71791
Product Number
1
Dosage Form
-
Strength
60MG
Approval Date
1987-07-15
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
90MG
Approval Date
1988-04-06
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
71977
Product Number
1
Dosage Form
-
Strength
90MG
Approval Date
1988-04-06
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
25MG;80MG
Approval Date
1986-10-01
Active Ingredient
HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Application Number
70705
Product Number
1
Dosage Form
-
Strength
25MG;80MG
Approval Date
1986-10-01
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Product Number
2
Dosage Form
-
Strength
25MG;40MG
Approval Date
1986-10-01
Active Ingredient
HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Application Number
70705
Product Number
2
Dosage Form
-
Strength
25MG;40MG
Approval Date
1986-10-01
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
25MG;80MG
Approval Date
1988-03-14
Active Ingredient
HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Application Number
72043
Product Number
1
Dosage Form
-
Strength
25MG;80MG
Approval Date
1988-03-14
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Product Number
2
Dosage Form
-
Strength
25MG;40MG
Approval Date
1988-03-14
Active Ingredient
HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Application Number
72043
Product Number
2
Dosage Form
-
Strength
25MG;40MG
Approval Date
1988-03-14
Regulatory Status
Discontinued
Drug Name
PROPYLTHIOURACIL
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Active Ingredient
PROPYLTHIOURACIL
Application Number
80215
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PURIFIED CORTROPHIN GEL
Product Number
1
Dosage Form
-
Strength
40 UNITS/ML
Approval Date
1982-01-01
Active Ingredient
CORTICOTROPIN
Application Number
8975
Product Number
1
Dosage Form
-
Strength
40 UNITS/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PYRIDOSTIGMINE BROMIDE
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
2005-07-20
Active Ingredient
PYRIDOSTIGMINE BROMIDE
Application Number
40512
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
2005-07-20
Regulatory Status
Discontinued
Drug Name
QUINAPRIL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE
Approval Date
2007-08-24
Active Ingredient
QUINAPRIL HYDROCHLORIDE
Application Number
75504
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE
Approval Date
2007-08-24
Regulatory Status
Discontinued
Drug Name
QUINAPRIL HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
2007-08-24
Active Ingredient
QUINAPRIL HYDROCHLORIDE
Application Number
75504
Product Number
2
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
2007-08-24
Regulatory Status
Discontinued
Drug Name
QUINAPRIL HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
EQ 20MG BASE
Approval Date
2007-08-24
Active Ingredient
QUINAPRIL HYDROCHLORIDE
Application Number
75504
Product Number
3
Dosage Form
-
Strength
EQ 20MG BASE
Approval Date
2007-08-24
Regulatory Status
Discontinued
Drug Name
QUINAPRIL HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
EQ 40MG BASE
Approval Date
2007-08-24
Active Ingredient
QUINAPRIL HYDROCHLORIDE
Application Number
75504
Product Number
4
Dosage Form
-
Strength
EQ 40MG BASE
Approval Date
2007-08-24
Regulatory Status
Discontinued
Drug Name
QUINIDINE GLUCONATE
Product Number
1
Dosage Form
-
Strength
324MG
Approval Date
1982-09-29
Active Ingredient
QUINIDINE GLUCONATE
Application Number
87810
Product Number
1
Dosage Form
-
Strength
324MG
Approval Date
1982-09-29
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
1997-07-31
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
74488
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
1997-07-31
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
1997-07-31
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
74488
Product Number
2
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
1997-07-31
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2000-01-14
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
75212
Product Number
1
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2000-01-14
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2000-01-14
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
75296
Product Number
1
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2000-01-14
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
2005-12-19
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
77426
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
2005-12-19
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
2005-12-19
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
77426
Product Number
2
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
2005-12-19
Regulatory Status
Discontinued
Drug Name
RANOLAZINE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
2019-10-29
Active Ingredient
RANOLAZINE
Application Number
210482
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
2019-10-29
Regulatory Status
Discontinued
Drug Name
RANOLAZINE
Product Number
2
Dosage Form
-
Strength
1GM
Approval Date
2019-10-29
Active Ingredient
RANOLAZINE
Application Number
210482
Product Number
2
Dosage Form
-
Strength
1GM
Approval Date
2019-10-29
Regulatory Status
Discontinued
Drug Name
ROSIGLITAZONE MALEATE
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2013-01-25
Active Ingredient
ROSIGLITAZONE MALEATE
Application Number
76747
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2013-01-25
Regulatory Status
Discontinued
Drug Name
ROSIGLITAZONE MALEATE
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2013-01-25
Active Ingredient
ROSIGLITAZONE MALEATE
Application Number
76747
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2013-01-25
Regulatory Status
Discontinued
Drug Name
ROSIGLITAZONE MALEATE
Product Number
3
Dosage Form
-
Strength
EQ 8MG BASE
Approval Date
2013-01-25
Active Ingredient
ROSIGLITAZONE MALEATE
Application Number
76747
Product Number
3
Dosage Form
-
Strength
EQ 8MG BASE
Approval Date
2013-01-25
Regulatory Status
Discontinued
Drug Name
SODIUM POLYSTYRENE SULFONATE
Product Number
1
Dosage Form
-
Strength
15GM/60ML
Approval Date
2011-05-13
Active Ingredient
SODIUM POLYSTYRENE SULFONATE
Application Number
90590
Product Number
1
Dosage Form
-
Strength
15GM/60ML
Approval Date
2011-05-13
Regulatory Status
Discontinued
Drug Name
SULFAMETHOXAZOLE AND TRIMETHOPRIM
Product Number
1
Dosage Form
-
Strength
200MG/5ML;40MG/5ML
Approval Date
1987-06-02
Active Ingredient
SULFAMETHOXAZOLE; TRIMETHOPRIM
Application Number
70028
Product Number
1
Dosage Form
-
Strength
200MG/5ML;40MG/5ML
Approval Date
1987-06-02
Regulatory Status
Discontinued
Drug Name
SULFISOXAZOLE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
SULFISOXAZOLE
Application Number
80142
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SULINDAC
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1992-02-28
Active Ingredient
SULINDAC
Application Number
72973
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1992-02-28
Regulatory Status
Discontinued
Drug Name
SULINDAC
Product Number
2
Dosage Form
-
Strength
150MG
Approval Date
1992-02-28
Active Ingredient
SULINDAC
Application Number
72973
Product Number
2
Dosage Form
-
Strength
150MG
Approval Date
1992-02-28
Regulatory Status
Discontinued
Drug Name
TEMOZOLOMIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2016-07-13
Active Ingredient
TEMOZOLOMIDE
Application Number
203490
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2016-07-13
Regulatory Status
Discontinued
Drug Name
TEMOZOLOMIDE
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
2016-07-13
Active Ingredient
TEMOZOLOMIDE
Application Number
203490
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
2016-07-13
Regulatory Status
Discontinued
Drug Name
TEMOZOLOMIDE
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2016-07-13
Active Ingredient
TEMOZOLOMIDE
Application Number
203490
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2016-07-13
Regulatory Status
Discontinued
Drug Name
TEMOZOLOMIDE
Product Number
4
Dosage Form
-
Strength
140MG
Approval Date
2016-07-13
Active Ingredient
TEMOZOLOMIDE
Application Number
203490
Product Number
4
Dosage Form
-
Strength
140MG
Approval Date
2016-07-13
Regulatory Status
Discontinued
Drug Name
TEMOZOLOMIDE
Product Number
5
Dosage Form
-
Strength
180MG
Approval Date
2016-07-13
Active Ingredient
TEMOZOLOMIDE
Application Number
203490
Product Number
5
Dosage Form
-
Strength
180MG
Approval Date
2016-07-13
Regulatory Status
Discontinued
Drug Name
TEMOZOLOMIDE
Product Number
6
Dosage Form
-
Strength
250MG
Approval Date
2016-07-13
Active Ingredient
TEMOZOLOMIDE
Application Number
203490
Product Number
6
Dosage Form
-
Strength
250MG
Approval Date
2016-07-13
Regulatory Status
Discontinued
Drug Name
TENUATE DOSPAN
Product Number
1
Dosage Form
-
Strength
75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DIETHYLPROPION HYDROCHLORIDE
Application Number
12546
Product Number
1
Dosage Form
-
Strength
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
TESTOSTERONE
Product Number
1
Dosage Form
-
Strength
25MG/2.5GM PACKET
Approval Date
2012-02-14
Active Ingredient
TESTOSTERONE
Application Number
202763
Product Number
1
Dosage Form
-
Strength
25MG/2.5GM PACKET
Approval Date
2012-02-14
Regulatory Status
Discontinued
Drug Name
TESTOSTERONE
Product Number
2
Dosage Form
-
Strength
50MG/5GM PACKET
Approval Date
2012-02-14
Active Ingredient
TESTOSTERONE
Application Number
202763
Product Number
2
Dosage Form
-
Strength
50MG/5GM PACKET
Approval Date
2012-02-14
Regulatory Status
Discontinued
Drug Name
TETRACYCLINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE HYDROCHLORIDE
Application Number
61471
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1983-04-14
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88194
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1983-04-14
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1983-04-14
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88270
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1983-04-14
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
1983-04-14
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88271
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
1983-04-14
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1983-04-14
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88272
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1983-04-14
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1983-10-03
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88273
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1983-10-03
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1985-05-17
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88456
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1985-05-17
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1985-05-17
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88493
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1985-05-17
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
1987-11-09
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
89602
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
1987-11-09
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1987-11-09
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
89603
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1987-11-09
Regulatory Status
Discontinued
Drug Name
TIMOLOL MALEATE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1991-07-31
Active Ingredient
TIMOLOL MALEATE
Application Number
72917
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1991-07-31
Regulatory Status
Discontinued
Drug Name
TIMOLOL MALEATE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1991-07-31
Active Ingredient
TIMOLOL MALEATE
Application Number
72918
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1991-07-31
Regulatory Status
Discontinued
Drug Name
TIMOLOL MALEATE
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1991-07-31
Active Ingredient
TIMOLOL MALEATE
Application Number
72919
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1991-07-31
Regulatory Status
Discontinued
Drug Name
TIZANIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2002-07-12
Active Ingredient
TIZANIDINE HYDROCHLORIDE
Application Number
76283
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2002-07-12
Regulatory Status
Discontinued
Drug Name
TIZANIDINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2002-07-12
Active Ingredient
TIZANIDINE HYDROCHLORIDE
Application Number
76283
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2002-07-12
Regulatory Status
Discontinued
Drug Name
TIZANIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2002-07-03
Active Ingredient
TIZANIDINE HYDROCHLORIDE
Application Number
76284
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2002-07-03
Regulatory Status
Discontinued
Drug Name
TIZANIDINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2002-07-03
Active Ingredient
TIZANIDINE HYDROCHLORIDE
Application Number
76284
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2002-07-03
Regulatory Status
Discontinued
Drug Name
TIZANIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2004-09-30
Active Ingredient
TIZANIDINE HYDROCHLORIDE
Application Number
76321
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2004-09-30
Regulatory Status
Discontinued
Drug Name
TIZANIDINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2004-09-30
Active Ingredient
TIZANIDINE HYDROCHLORIDE
Application Number
76321
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2004-09-30
Regulatory Status
Discontinued
Drug Name
TIZANIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2003-04-09
Active Ingredient
TIZANIDINE HYDROCHLORIDE
Application Number
76371
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2003-04-09
Regulatory Status
Discontinued
Drug Name
TIZANIDINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2003-04-09
Active Ingredient
TIZANIDINE HYDROCHLORIDE
Application Number
76371
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE
Approval Date
2003-04-09
Regulatory Status
Discontinued
Drug Name
TOLBUTAMIDE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
TOLBUTAMIDE
Application Number
87093
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TOLMETIN SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 400MG BASE
Approval Date
1992-01-24
Active Ingredient
TOLMETIN SODIUM
Application Number
73308
Product Number
1
Dosage Form
-
Strength
EQ 400MG BASE
Approval Date
1992-01-24
Regulatory Status
Discontinued
Drug Name
TOLMETIN SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 400MG BASE
Approval Date
1992-01-24
Active Ingredient
TOLMETIN SODIUM
Application Number
73392
Product Number
1
Dosage Form
-
Strength
EQ 400MG BASE
Approval Date
1992-01-24
Regulatory Status
Discontinued
Drug Name
TOLMETIN SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 400MG BASE
Approval Date
1992-05-29
Active Ingredient
TOLMETIN SODIUM
Application Number
73519
Product Number
1
Dosage Form
-
Strength
EQ 400MG BASE
Approval Date
1992-05-29
Regulatory Status
Discontinued
Drug Name
TOLMETIN SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 600MG BASE
Approval Date
1992-06-30
Active Ingredient
TOLMETIN SODIUM
Application Number
73527
Product Number
1
Dosage Form
-
Strength
EQ 600MG BASE
Approval Date
1992-06-30
Regulatory Status
Discontinued
Drug Name
TRIAMTERENE AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
50MG;75MG
Approval Date
1996-01-31
Active Ingredient
HYDROCHLOROTHIAZIDE; TRIAMTERENE
Application Number
73467
Product Number
1
Dosage Form
-
Strength
50MG;75MG
Approval Date
1996-01-31
Regulatory Status
Discontinued
Drug Name
TRIAMTERENE AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
25MG;50MG
Approval Date
1995-03-30
Active Ingredient
HYDROCHLOROTHIAZIDE; TRIAMTERENE
Application Number
74259
Product Number
1
Dosage Form
-
Strength
25MG;50MG
Approval Date
1995-03-30
Regulatory Status
Discontinued
Drug Name
TRIAMTERENE AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
25MG;37.5MG
Approval Date
1998-01-06
Active Ingredient
HYDROCHLOROTHIAZIDE; TRIAMTERENE
Application Number
74970
Product Number
1
Dosage Form
-
Strength
25MG;37.5MG
Approval Date
1998-01-06
Regulatory Status
Discontinued
Drug Name
VANCOCIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/6ML
Approval Date
1982-01-01
Active Ingredient
VANCOMYCIN HYDROCHLORIDE
Application Number
61667
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/6ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ZOLMITRIPTAN
Product Number
1
Dosage Form
-
Strength
2.5MG
Approval Date
2014-03-04
Active Ingredient
ZOLMITRIPTAN
Application Number
90861
Product Number
1
Dosage Form
-
Strength
2.5MG
Approval Date
2014-03-04
Regulatory Status
Discontinued
Drug Name
ZOLMITRIPTAN
Product Number
2
Dosage Form
-
Strength
5MG
Approval Date
2014-03-04
Active Ingredient
ZOLMITRIPTAN
Application Number
90861
Product Number
2
Dosage Form
-
Strength
5MG
Approval Date
2014-03-04
Regulatory Status
Discontinued
Drug Name
ZONISAMIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2005-12-22
Active Ingredient
ZONISAMIDE
Application Number
77639
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
77639
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
77639
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2005-12-22
Regulatory Status
Discontinued
Drug Name
ZONISAMIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
2005-12-22
Active Ingredient
ZONISAMIDE
Application Number
77641
Product Number
1
Dosage Form
-
Strength
100MG
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
77641
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2005-12-22
Regulatory Status
Discontinued
Drug Name
ZONISAMIDE
Product Number
3
Dosage Form
-
Strength
25MG
Approval Date
2005-12-22
Active Ingredient
ZONISAMIDE
Application Number
77641
Product Number
3
Dosage Form
-
Strength
25MG
Approval Date
2005-12-22
Regulatory Status
Discontinued
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Drug Status Breakdown
331 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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Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Application Number
88629
Product Number
1
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form
-
Strength
300MG;60MG
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