Barr Laboratories Inc. Discontinued
FDA Approved Drugs

Barr Laboratories 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.

Discontinued
  • Total Records 165
  • Latest Approval Date Apr 26, 2017
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
269
View
Unclassified
16
View
Discontinued
165
View
OTC
1
View
RX
87
View
Company Overview

Company

Barr Laboratories Inc. Discontinued

Country

U.S.A

Website

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Company Snapshot

Barr Laboratories Inc. Discontinued

225 Summit Ave, Montvale, NJ 07645

U.S.A

www.barrlabs.com View on Map
FDA Approved Drug Records ( 165 records )
2013
18 Nov
Discontinued Application: 200143

Drug Name

ACAMPROSATE CALCIUM

Product Number

1

Dosage Form

-

Strength

333MG

Approval Date

2013-11-18

200143 / 1

Active Ingredient

ACAMPROSATE CALCIUM

Application Number

200143

Product Number

1

Dosage Form

-

Strength

333MG

Approval Date

2013-11-18

Regulatory Status

Discontinued

1983
19 Aug
Discontinued Application: 88297

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-08-19

88297 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

88297

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-08-19

Regulatory Status

Discontinued

1983
19 Aug
Discontinued Application: 88298

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1983-08-19

88298 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

88298

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1983-08-19

Regulatory Status

Discontinued

2004
22 Apr
Discontinued Application: 76198

Drug Name

BALZIVA-21

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG

Approval Date

2004-04-22

76198 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

76198

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG

Approval Date

2004-04-22

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84468

Drug Name

BROMPHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

84468 / 1

Active Ingredient

BROMPHENIRAMINE MALEATE

Application Number

84468

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2014
02 Apr
Discontinued Application: 90379

Drug Name

BUDESONIDE

Product Number

1

Dosage Form

-

Strength

3MG

Approval Date

2014-04-02

90379 / 1

Active Ingredient

BUDESONIDE

Application Number

90379

Product Number

1

Dosage Form

-

Strength

3MG

Approval Date

2014-04-02

Regulatory Status

Discontinued

2010
07 May
Discontinued Application: 90360

Drug Name

BUPRENORPHINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2010-05-07

90360 / 1

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE

Application Number

90360

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2010-05-07

Regulatory Status

Discontinued

2010
07 May
Discontinued Application: 90360

Drug Name

BUPRENORPHINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2010-05-07

90360 / 2

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE

Application Number

90360

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2010-05-07

Regulatory Status

Discontinued

1987
26 Jun
Discontinued Application: 62773

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1987-06-26

62773 / 1

Active Ingredient

CEPHALEXIN

Application Number

62773

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1987-06-26

Regulatory Status

Discontinued

1987
22 Apr
Discontinued Application: 62775

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1987-04-22

62775 / 1

Active Ingredient

CEPHALEXIN

Application Number

62775

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1987-04-22

Regulatory Status

Discontinued

1987
06 Aug
Discontinued Application: 62777

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1987-08-06

62777 / 1

Active Ingredient

CEPHALEXIN

Application Number

62777

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1987-08-06

Regulatory Status

Discontinued

1987
06 Aug
Discontinued Application: 62778

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1987-08-06

62778 / 1

Active Ingredient

CEPHALEXIN

Application Number

62778

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1987-08-06

Regulatory Status

Discontinued

1987
17 Aug
Discontinued Application: 62826

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1987-08-17

62826 / 1

Active Ingredient

CEPHALEXIN

Application Number

62826

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1987-08-17

Regulatory Status

Discontinued

1987
17 Aug
Discontinued Application: 62827

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1987-08-17

62827 / 1

Active Ingredient

CEPHALEXIN

Application Number

62827

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1987-08-17

Regulatory Status

Discontinued

1988
22 Apr
Discontinued Application: 62850

Drug Name

CEPHRADINE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1988-04-22

62850 / 1

Active Ingredient

CEPHRADINE

Application Number

62850

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1988-04-22

Regulatory Status

Discontinued

1988
22 Apr
Discontinued Application: 62851

Drug Name

CEPHRADINE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1988-04-22

62851 / 1

Active Ingredient

CEPHRADINE

Application Number

62851

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1988-04-22

Regulatory Status

Discontinued

1988
19 May
Discontinued Application: 62858

Drug Name

CEPHRADINE

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1988-05-19

62858 / 1

Active Ingredient

CEPHRADINE

Application Number

62858

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1988-05-19

Regulatory Status

Discontinued

1988
19 May
Discontinued Application: 62859

Drug Name

CEPHRADINE

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

1988-05-19

62859 / 1

Active Ingredient

CEPHRADINE

Application Number

62859

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

1988-05-19

Regulatory Status

Discontinued

1985
19 Sep
Discontinued Application: 88902

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-09-19

88902 / 1

Active Ingredient

CHLORTHALIDONE

Application Number

88902

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-09-19

Regulatory Status

Discontinued

1985
19 Sep
Discontinued Application: 88903

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1985-09-19

88903 / 1

Active Ingredient

CHLORTHALIDONE

Application Number

88903

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1985-09-19

Regulatory Status

Discontinued

1988
04 May
Discontinued Application: 89895

Drug Name

CHLORZOXAZONE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1988-05-04

89895 / 1

Active Ingredient

CHLORZOXAZONE

Application Number

89895

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1988-05-04

Regulatory Status

Discontinued

2004
09 Jun
Discontinued Application: 74124

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-06-09

74124 / 1

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

74124

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-06-09

Regulatory Status

Discontinued

2004
09 Jun
Discontinued Application: 74124

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-06-09

74124 / 2

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

74124

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-06-09

Regulatory Status

Discontinued

2004
09 Jun
Discontinued Application: 74124

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

74124 / 3

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

74124

Product Number

3

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83471

Drug Name

CORTISONE ACETATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

83471 / 1

Active Ingredient

CORTISONE ACETATE

Application Number

83471

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2004
13 Dec
Discontinued Application: 65171

Drug Name

DEMECLOCYCLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2004-12-13

65171 / 1

Active Ingredient

DEMECLOCYCLINE HYDROCHLORIDE

Application Number

65171

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2004-12-13

Regulatory Status

Discontinued

2004
13 Dec
Discontinued Application: 65171

Drug Name

DEMECLOCYCLINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2004-12-13

65171 / 2

Active Ingredient

DEMECLOCYCLINE HYDROCHLORIDE

Application Number

65171

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2004-12-13

Regulatory Status

Discontinued

2013
12 Feb
Discontinued Application: 76536

Drug Name

DEXTROAMP SACCHARATE,AMP ASPARTATE,DEXTROAMP SULFATE AND AMP SULFATE

Product Number

1

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG

Approval Date

2013-02-12

76536 / 1

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

76536

Product Number

1

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG

Approval Date

2013-02-12

Regulatory Status

Discontinued

2013
12 Feb
Discontinued Application: 76536

Drug Name

DEXTROAMP SACCHARATE,AMP ASPARTATE,DEXTROAMP SULFATE AND AMP SULFATE

Product Number

2

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG

Approval Date

2013-02-12

76536 / 2

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

76536

Product Number

2

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG

Approval Date

2013-02-12

Regulatory Status

Discontinued

2013
12 Feb
Discontinued Application: 76536

Drug Name

DEXTROAMP SACCHARATE,AMP ASPARTATE,DEXTROAMP SULFATE AND AMP SULFATE

Product Number

3

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG

Approval Date

2013-02-12

76536 / 3

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

76536

Product Number

3

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG

Approval Date

2013-02-12

Regulatory Status

Discontinued

2013
12 Feb
Discontinued Application: 76536

Drug Name

DEXTROAMP SACCHARATE,AMP ASPARTATE,DEXTROAMP SULFATE AND AMP SULFATE

Product Number

4

Dosage Form

-

Strength

5MG;5MG;5MG;5MG

Approval Date

2013-02-12

76536 / 4

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

76536

Product Number

4

Dosage Form

-

Strength

5MG;5MG;5MG;5MG

Approval Date

2013-02-12

Regulatory Status

Discontinued

2013
12 Feb
Discontinued Application: 76536

Drug Name

DEXTROAMP SACCHARATE,AMP ASPARTATE,DEXTROAMP SULFATE AND AMP SULFATE

Product Number

5

Dosage Form

-

Strength

6.25MG;6.25MG;6.25MG;6.25MG

Approval Date

2013-02-12

76536 / 5

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

76536

Product Number

5

Dosage Form

-

Strength

6.25MG;6.25MG;6.25MG;6.25MG

Approval Date

2013-02-12

Regulatory Status

Discontinued

2013
12 Feb
Discontinued Application: 76536

Drug Name

DEXTROAMP SACCHARATE,AMP ASPARTATE,DEXTROAMP SULFATE AND AMP SULFATE

Product Number

6

Dosage Form

-

Strength

7.5MG;7.5MG;7.5MG;7.5MG

Approval Date

2013-02-12

76536 / 6

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

76536

Product Number

6

Dosage Form

-

Strength

7.5MG;7.5MG;7.5MG;7.5MG

Approval Date

2013-02-12

Regulatory Status

Discontinued

1985
01 Nov
Discontinued Application: 70152

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1985-11-01

70152 / 1

Active Ingredient

DIAZEPAM

Application Number

70152

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1985-11-01

Regulatory Status

Discontinued

1985
01 Nov
Discontinued Application: 70154

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1985-11-01

70154 / 1

Active Ingredient

DIAZEPAM

Application Number

70154

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1985-11-01

Regulatory Status

Discontinued

2004
03 Dec
Discontinued Application: 77167

Drug Name

DIDANOSINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2004-12-03

77167 / 1

Active Ingredient

DIDANOSINE

Application Number

77167

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2004-12-03

Regulatory Status

Discontinued

2004
03 Dec
Discontinued Application: 77167

Drug Name

DIDANOSINE

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

2004-12-03

77167 / 2

Active Ingredient

DIDANOSINE

Application Number

77167

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

2004-12-03

Regulatory Status

Discontinued

2004
03 Dec
Discontinued Application: 77167

Drug Name

DIDANOSINE

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2004-12-03

77167 / 3

Active Ingredient

DIDANOSINE

Application Number

77167

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2004-12-03

Regulatory Status

Discontinued

2008
09 May
Discontinued Application: 77527

Drug Name

DROSPIRENONE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

3MG;0.03MG

Approval Date

2008-05-09

77527 / 1

Active Ingredient

DROSPIRENONE; ETHINYL ESTRADIOL

Application Number

77527

Product Number

1

Dosage Form

-

Strength

3MG;0.03MG

Approval Date

2008-05-09

Regulatory Status

Discontinued

2009
30 Mar
Discontinued Application: 78515

Drug Name

DROSPIRENONE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

3MG;0.02MG

Approval Date

2009-03-30

78515 / 1

Active Ingredient

DROSPIRENONE; ETHINYL ESTRADIOL

Application Number

78515

Product Number

1

Dosage Form

-

Strength

3MG;0.02MG

Approval Date

2009-03-30

Regulatory Status

Discontinued

1988
25 Nov
Discontinued Application: 62999

Drug Name

E-BASE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1988-11-25

62999 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

62999

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1988-11-25

Regulatory Status

Discontinued

1990
15 May
Discontinued Application: 63028

Drug Name

E-BASE

Product Number

1

Dosage Form

-

Strength

333MG

Approval Date

1990-05-15

63028 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

63028

Product Number

1

Dosage Form

-

Strength

333MG

Approval Date

1990-05-15

Regulatory Status

Discontinued

1990
15 May
Discontinued Application: 63086

Drug Name

E-BASE

Product Number

1

Dosage Form

-

Strength

333MG

Approval Date

1990-05-15

63086 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

63086

Product Number

1

Dosage Form

-

Strength

333MG

Approval Date

1990-05-15

Regulatory Status

Discontinued

1989
04 May
Discontinued Application: 63098

Drug Name

ERYTHROMYCIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1989-05-04

63098 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

63098

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1989-05-04

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62162

Drug Name

ERYTHROMYCIN ESTOLATE

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE

Approval Date

1982-01-01

62162 / 1

Active Ingredient

ERYTHROMYCIN ESTOLATE

Application Number

62162

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62162

Drug Name

ERYTHROMYCIN ESTOLATE

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

62162 / 2

Active Ingredient

ERYTHROMYCIN ESTOLATE

Application Number

62162

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62256

Drug Name

ERYTHROMYCIN ETHYLSUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 400MG BASE

Approval Date

1982-01-01

62256 / 1

Active Ingredient

ERYTHROMYCIN ETHYLSUCCINATE

Application Number

62256

Product Number

1

Dosage Form

-

Strength

EQ 400MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988
20 May
Discontinued Application: 62759

Drug Name

ERYTHROMYCIN ETHYLSUCCINATE AND SULFISOXAZOLE ACETYL

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/5ML;EQ 600MG BASE/5ML

Approval Date

1988-05-20

62759 / 1

Active Ingredient

ERYTHROMYCIN ETHYLSUCCINATE; SULFISOXAZOLE ACETYL

Application Number

62759

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/5ML;EQ 600MG BASE/5ML

Approval Date

1988-05-20

Regulatory Status

Discontinued

2005
29 Apr
Discontinued Application: 76812

Drug Name

ESTRADIOL AND NORGESTIMATE

Product Number

1

Dosage Form

-

Strength

1MG,1MG;N/A,0.09MG

Approval Date

2005-04-29

76812 / 1

Active Ingredient

ESTRADIOL; NORGESTIMATE

Application Number

76812

Product Number

1

Dosage Form

-

Strength

1MG,1MG;N/A,0.09MG

Approval Date

2005-04-29

Regulatory Status

Discontinued

1996
27 Nov
Discontinued Application: 40135

Drug Name

ESTROPIPATE

Product Number

1

Dosage Form

-

Strength

0.75MG

Approval Date

1996-11-27

40135 / 1

Active Ingredient

ESTROPIPATE

Application Number

40135

Product Number

1

Dosage Form

-

Strength

0.75MG

Approval Date

1996-11-27

Regulatory Status

Discontinued

1996
27 Nov
Discontinued Application: 40135

Drug Name

ESTROPIPATE

Product Number

2

Dosage Form

-

Strength

1.5MG

Approval Date

1996-11-27

40135 / 2

Active Ingredient

ESTROPIPATE

Application Number

40135

Product Number

2

Dosage Form

-

Strength

1.5MG

Approval Date

1996-11-27

Regulatory Status

Discontinued

1996
27 Nov
Discontinued Application: 40135

Drug Name

ESTROPIPATE

Product Number

3

Dosage Form

-

Strength

3MG

Approval Date

1996-11-27

40135 / 3

Active Ingredient

ESTROPIPATE

Application Number

40135

Product Number

3

Dosage Form

-

Strength

3MG

Approval Date

1996-11-27

Regulatory Status

Discontinued

2001
26 Nov
Discontinued Application: 76057

Drug Name

ETHAMBUTOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

2001-11-26

76057 / 1

Active Ingredient

ETHAMBUTOL HYDROCHLORIDE

Application Number

76057

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

2001-11-26

Regulatory Status

Discontinued

2005
13 Jul
Discontinued Application: 76169

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

2005-07-13

76169 / 1

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76169

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

2005-07-13

Regulatory Status

Discontinued

2005
31 Aug
Discontinued Application: 76191

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2005-08-31

76191 / 1

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76191

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2005-08-31

Regulatory Status

Discontinued

2005
31 Aug
Discontinued Application: 76191

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

2005-08-31

76191 / 2

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76191

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

2005-08-31

Regulatory Status

Discontinued

2005
31 Aug
Discontinued Application: 76191

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

180MG

Approval Date

2005-08-31

76191 / 3

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76191

Product Number

3

Dosage Form

-

Strength

180MG

Approval Date

2005-08-31

Regulatory Status

Discontinued

2005
14 Apr
Discontinued Application: 76236

Drug Name

FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

60MG;120MG

Approval Date

2005-04-14

76236 / 1

Active Ingredient

FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

Application Number

76236

Product Number

1

Dosage Form

-

Strength

60MG;120MG

Approval Date

2005-04-14

Regulatory Status

Discontinued

2003
21 Jan
Discontinued Application: 40425

Drug Name

FLUDROCORTISONE ACETATE

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

2003-01-21

40425 / 1

Active Ingredient

FLUDROCORTISONE ACETATE

Application Number

40425

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

2003-01-21

Regulatory Status

Discontinued

2001
02 Aug
Discontinued Application: 74803

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2001-08-02

74803 / 1

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

74803

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2001-08-02

Regulatory Status

Discontinued

2002
30 Jan
Discontinued Application: 74803

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-30

74803 / 2

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

74803

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-30

Regulatory Status

Discontinued

2002
01 Feb
Discontinued Application: 75810

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-02-01

75810 / 1

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75810

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-02-01

Regulatory Status

Discontinued

2010
24 Mar
Discontinued Application: 76237

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 90MG BASE

Approval Date

2010-03-24

76237 / 1

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

76237

Product Number

1

Dosage Form

-

Strength

EQ 90MG BASE

Approval Date

2010-03-24

Regulatory Status

Discontinued

2005
18 May
Discontinued Application: 76251

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2005-05-18

76251 / 1

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

76251

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2005-05-18

Regulatory Status

Discontinued

1986
08 Jan
Discontinued Application: 89177

Drug Name

FOLIC ACID

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1986-01-08

89177 / 1

Active Ingredient

FOLIC ACID

Application Number

89177

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1986-01-08

Regulatory Status

Discontinued

1992
28 Feb
Discontinued Application: 72694

Drug Name

GENCEPT 10/11-21

Product Number

1

Dosage Form

-

Strength

0.035MG,0.035MG;0.5MG,1MG

Approval Date

1992-02-28

72694 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

72694

Product Number

1

Dosage Form

-

Strength

0.035MG,0.035MG;0.5MG,1MG

Approval Date

1992-02-28

Regulatory Status

Discontinued

1997
04 Apr
Discontinued Application: 74619

Drug Name

GLIPIZIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1997-04-04

74619 / 1

Active Ingredient

GLIPIZIDE

Application Number

74619

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1997-04-04

Regulatory Status

Discontinued

1997
04 Apr
Discontinued Application: 74619

Drug Name

GLIPIZIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1997-04-04

74619 / 2

Active Ingredient

GLIPIZIDE

Application Number

74619

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1997-04-04

Regulatory Status

Discontinued

2007
31 Dec
Discontinued Application: 78221

Drug Name

GRANISETRON HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2007-12-31

78221 / 1

Active Ingredient

GRANISETRON HYDROCHLORIDE

Application Number

78221

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2007-12-31

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84771

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

84771 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

84771

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2000
26 Jul
Discontinued Application: 40307

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;2.5MG

Approval Date

2000-07-26

40307 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40307

Product Number

1

Dosage Form

-

Strength

500MG;2.5MG

Approval Date

2000-07-26

Regulatory Status

Discontinued

2000
26 Jul
Discontinued Application: 40307

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

2000-07-26

40307 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40307

Product Number

2

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

2000-07-26

Regulatory Status

Discontinued

2000
26 Jul
Discontinued Application: 40307

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

3

Dosage Form

-

Strength

650MG;7.5MG

Approval Date

2000-07-26

40307 / 3

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40307

Product Number

3

Dosage Form

-

Strength

650MG;7.5MG

Approval Date

2000-07-26

Regulatory Status

Discontinued

2000
26 Jul
Discontinued Application: 40307

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

4

Dosage Form

-

Strength

650MG;10MG

Approval Date

2000-07-26

40307 / 4

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40307

Product Number

4

Dosage Form

-

Strength

650MG;10MG

Approval Date

2000-07-26

Regulatory Status

Discontinued

2000
26 Jul
Discontinued Application: 40308

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

2000-07-26

40308 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40308

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

2000-07-26

Regulatory Status

Discontinued

2000
26 Jul
Discontinued Application: 40308

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

750MG;7.5MG

Approval Date

2000-07-26

40308 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40308

Product Number

2

Dosage Form

-

Strength

750MG;7.5MG

Approval Date

2000-07-26

Regulatory Status

Discontinued

2000
26 Jul
Discontinued Application: 40309

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;10MG

Approval Date

2000-07-26

40309 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40309

Product Number

1

Dosage Form

-

Strength

500MG;10MG

Approval Date

2000-07-26

Regulatory Status

Discontinued

1984
21 Dec
Discontinued Application: 88577

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1984-12-21

88577 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

88577

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1984-12-21

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83999

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

83999 / 1

Active Ingredient

HYDROCORTISONE

Application Number

83999

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2003
25 Apr
Discontinued Application: 76444

Drug Name

HYDROMORPHONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

2003-04-25

76444 / 1

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

76444

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

2003-04-25

Regulatory Status

Discontinued

1998
30 Jul
Discontinued Application: 75020

Drug Name

HYDROXYUREA

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1998-07-30

75020 / 1

Active Ingredient

HYDROXYUREA

Application Number

75020

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1998-07-30

Regulatory Status

Discontinued

2000
26 Jun
Discontinued Application: 75020

Drug Name

HYDROXYUREA

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

2000-06-26

75020 / 2

Active Ingredient

HYDROXYUREA

Application Number

75020

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

2000-06-26

Regulatory Status

Discontinued

2000
21 Sep
Discontinued Application: 75143

Drug Name

HYDROXYUREA

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

2000-09-21

75143 / 2

Active Ingredient

HYDROXYUREA

Application Number

75143

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

2000-09-21

Regulatory Status

Discontinued

2000
29 Aug
Discontinued Application: 75734

Drug Name

HYDROXYUREA

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

2000-08-29

75734 / 1

Active Ingredient

HYDROXYUREA

Application Number

75734

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

2000-08-29

Regulatory Status

Discontinued

2005
13 Sep
Discontinued Application: 77083

Drug Name

LEFLUNOMIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2005-09-13

77083 / 1

Active Ingredient

LEFLUNOMIDE

Application Number

77083

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2005-09-13

Regulatory Status

Discontinued

2005
13 Sep
Discontinued Application: 77083

Drug Name

LEFLUNOMIDE

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2005-09-13

77083 / 2

Active Ingredient

LEFLUNOMIDE

Application Number

77083

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2005-09-13

Regulatory Status

Discontinued

2002
20 Mar
Discontinued Application: 75803

Drug Name

LESSINA-21

Product Number

1

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2002-03-20

75803 / 1

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

75803

Product Number

1

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2002-03-20

Regulatory Status

Discontinued

2003
29 Apr
Discontinued Application: 75862

Drug Name

LEVONORGESTREL AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2003-04-29

75862 / 1

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

75862

Product Number

1

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2003-04-29

Regulatory Status

Discontinued

2003
29 Apr
Discontinued Application: 75862

Drug Name

LEVONORGESTREL AND ETHINYL ESTRADIOL

Product Number

2

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2003-04-29

75862 / 2

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

75862

Product Number

2

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2003-04-29

Regulatory Status

Discontinued

1989
20 Mar
Discontinued Application: 72809

Drug Name

MECLOFENAMATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1989-03-20

72809 / 1

Active Ingredient

MECLOFENAMATE SODIUM

Application Number

72809

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1989-03-20

Regulatory Status

Discontinued

1989
20 Mar
Discontinued Application: 72848

Drug Name

MECLOFENAMATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1989-03-20

72848 / 1

Active Ingredient

MECLOFENAMATE SODIUM

Application Number

72848

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1989-03-20

Regulatory Status

Discontinued

1984
02 Jul
Discontinued Application: 88639

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1984-07-02

88639 / 1

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

88639

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1984-07-02

Regulatory Status

Discontinued

1984
19 Sep
Discontinued Application: 88640

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1984-09-19

88640 / 1

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

88640

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1984-09-19

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84230

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1982-01-01

84230 / 1

Active Ingredient

MEPROBAMATE

Application Number

84230

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2002
25 Jan
Discontinued Application: 75971

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2002-01-25

75971 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

75971

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2002-01-25

Regulatory Status

Discontinued

2002
25 Jan
Discontinued Application: 75971

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2002-01-25

75971 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

75971

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2002-01-25

Regulatory Status

Discontinued

2002
25 Jan
Discontinued Application: 75971

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2002-01-25

75971 / 3

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

75971

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2002-01-25

Regulatory Status

Discontinued

2005
25 Nov
Discontinued Application: 76496

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2005-11-25

76496 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

76496

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2005-11-25

Regulatory Status

Discontinued

2004
14 Oct
Discontinued Application: 76863

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

2004-10-14

76863 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

76863

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

2004-10-14

Regulatory Status

Discontinued

2012
13 Jul
Discontinued Application: 79031

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2012-07-13

79031 / 1

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

79031

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2012-07-13

Regulatory Status

Discontinued

2012
13 Jul
Discontinued Application: 79031

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2012-07-13

79031 / 2

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

79031

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2012-07-13

Regulatory Status

Discontinued

2012
13 Jul
Discontinued Application: 79031

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

40MG

Approval Date

2012-07-13

79031 / 3

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

79031

Product Number

3

Dosage Form

-

Strength

40MG

Approval Date

2012-07-13

Regulatory Status

Discontinued

2014
15 Oct
Discontinued Application: 79031

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

2014-10-15

79031 / 4

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

79031

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

2014-10-15

Regulatory Status

Discontinued

2009
17 Mar
Discontinued Application: 65485

Drug Name

MINOCYCLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 45MG BASE

Approval Date

2009-03-17

65485 / 1

Active Ingredient

MINOCYCLINE HYDROCHLORIDE

Application Number

65485

Product Number

1

Dosage Form

-

Strength

EQ 45MG BASE

Approval Date

2009-03-17

Regulatory Status

Discontinued

2009
17 Mar
Discontinued Application: 65485

Drug Name

MINOCYCLINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 90MG BASE

Approval Date

2009-03-17

65485 / 2

Active Ingredient

MINOCYCLINE HYDROCHLORIDE

Application Number

65485

Product Number

2

Dosage Form

-

Strength

EQ 90MG BASE

Approval Date

2009-03-17

Regulatory Status

Discontinued

2009
17 Mar
Discontinued Application: 65485

Drug Name

MINOCYCLINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 135MG BASE

Approval Date

2009-03-17

65485 / 3

Active Ingredient

MINOCYCLINE HYDROCHLORIDE

Application Number

65485

Product Number

3

Dosage Form

-

Strength

EQ 135MG BASE

Approval Date

2009-03-17

Regulatory Status

Discontinued

2012
18 May
Discontinued Application: 65485

Drug Name

MINOCYCLINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 65MG BASE

Approval Date

2012-05-18

65485 / 4

Active Ingredient

MINOCYCLINE HYDROCHLORIDE

Application Number

65485

Product Number

4

Dosage Form

-

Strength

EQ 65MG BASE

Approval Date

2012-05-18

Regulatory Status

Discontinued

2012
18 May
Discontinued Application: 65485

Drug Name

MINOCYCLINE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

EQ 115MG BASE

Approval Date

2012-05-18

65485 / 5

Active Ingredient

MINOCYCLINE HYDROCHLORIDE

Application Number

65485

Product Number

5

Dosage Form

-

Strength

EQ 115MG BASE

Approval Date

2012-05-18

Regulatory Status

Discontinued

2017
26 Apr
Discontinued Application: 65485

Drug Name

MINOCYCLINE HYDROCHLORIDE

Product Number

7

Dosage Form

-

Strength

EQ 80MG BASE

Approval Date

2017-04-26

65485 / 7

Active Ingredient

MINOCYCLINE HYDROCHLORIDE

Application Number

65485

Product Number

7

Dosage Form

-

Strength

EQ 80MG BASE

Approval Date

2017-04-26

Regulatory Status

Discontinued

2017
26 Apr
Discontinued Application: 65485

Drug Name

MINOCYCLINE HYDROCHLORIDE

Product Number

8

Dosage Form

-

Strength

EQ 105MG BASE

Approval Date

2017-04-26

65485 / 8

Active Ingredient

MINOCYCLINE HYDROCHLORIDE

Application Number

65485

Product Number

8

Dosage Form

-

Strength

EQ 105MG BASE

Approval Date

2017-04-26

Regulatory Status

Discontinued

1992
28 Feb
Discontinued Application: 72692

Drug Name

NORTREL 0.5/35-21

Product Number

1

Dosage Form

-

Strength

0.035MG;0.5MG

Approval Date

1992-02-28

72692 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

72692

Product Number

1

Dosage Form

-

Strength

0.035MG;0.5MG

Approval Date

1992-02-28

Regulatory Status

Discontinued

2007
25 Jun
Discontinued Application: 76693

Drug Name

ONDANSETRON

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2007-06-25

76693 / 1

Active Ingredient

ONDANSETRON

Application Number

76693

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2007-06-25

Regulatory Status

Discontinued

2007
25 Jun
Discontinued Application: 76693

Drug Name

ONDANSETRON

Product Number

2

Dosage Form

-

Strength

8MG

Approval Date

2007-06-25

76693 / 2

Active Ingredient

ONDANSETRON

Application Number

76693

Product Number

2

Dosage Form

-

Strength

8MG

Approval Date

2007-06-25

Regulatory Status

Discontinued

2014
04 Mar
Discontinued Application: 90526

Drug Name

OXYBUTYNIN

Product Number

1

Dosage Form

-

Strength

3.9MG/24HR

Approval Date

2014-03-04

90526 / 1

Active Ingredient

OXYBUTYNIN

Application Number

90526

Product Number

1

Dosage Form

-

Strength

3.9MG/24HR

Approval Date

2014-03-04

Regulatory Status

Discontinued

2000
02 Oct
Discontinued Application: 40304

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

2000-10-02

40304 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40304

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

2000-10-02

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87406

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

325MG;5MG

Approval Date

1982-01-01

87406 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

87406

Product Number

1

Dosage Form

-

Strength

325MG;5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2007
29 Nov
Discontinued Application: 78316

Drug Name

OXYCODONE HYDROCHLORIDE AND IBUPROFEN

Product Number

1

Dosage Form

-

Strength

400MG;5MG

Approval Date

2007-11-29

78316 / 1

Active Ingredient

IBUPROFEN; OXYCODONE HYDROCHLORIDE

Application Number

78316

Product Number

1

Dosage Form

-

Strength

400MG;5MG

Approval Date

2007-11-29

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83644

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

83644 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

83644

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83684

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

83684 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

83684

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83686

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

83686 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

83686

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83687

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

83687 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

83687

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84831

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

84831 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

84831

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84834

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

84834 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

84834

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84835

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

84835 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

84835

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2009
31 Aug
Discontinued Application: 90470

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

2009-08-31

90470 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

90470

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

2009-08-31

Regulatory Status

Discontinued

2010
18 Mar
Discontinued Application: 90591

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2010-03-18

90591 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

90591

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2010-03-18

Regulatory Status

Discontinued

2010
18 Mar
Discontinued Application: 90591

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2010-03-18

90591 / 2

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

90591

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2010-03-18

Regulatory Status

Discontinued

2002
23 May
Discontinued Application: 75866

Drug Name

PORTIA-21

Product Number

1

Dosage Form

-

Strength

0.03MG;0.15MG

Approval Date

2002-05-23

75866 / 1

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

75866

Product Number

1

Dosage Form

-

Strength

0.03MG;0.15MG

Approval Date

2002-05-23

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84426

Drug Name

PREDNISOLONE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

84426 / 2

Active Ingredient

PREDNISOLONE

Application Number

84426

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84177

Drug Name

QUINIDINE SULFATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

84177 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

84177

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80721

Drug Name

RESERPINE

Product Number

2

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

80721 / 2

Active Ingredient

RESERPINE

Application Number

80721

Product Number

2

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84579

Drug Name

RESERPINE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

50MG;0.125MG

Approval Date

1982-01-01

84579 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; RESERPINE

Application Number

84579

Product Number

1

Dosage Form

-

Strength

50MG;0.125MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84580

Drug Name

RESERPINE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;0.125MG

Approval Date

1982-01-01

84580 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; RESERPINE

Application Number

84580

Product Number

1

Dosage Form

-

Strength

25MG;0.125MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84225

Drug Name

SECOBARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

84225 / 1

Active Ingredient

SECOBARBITAL SODIUM

Application Number

84225

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983
25 Jul
Discontinued Application: 87189

Drug Name

SULFAMETHOXAZOLE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1983-07-25

87189 / 1

Active Ingredient

SULFAMETHOXAZOLE

Application Number

87189

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1983-07-25

Regulatory Status

Discontinued

1982
17 Sep
Discontinued Application: 87665

Drug Name

SULFINPYRAZONE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-09-17

87665 / 1

Active Ingredient

SULFINPYRAZONE

Application Number

87665

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-09-17

Regulatory Status

Discontinued

1982
17 Sep
Discontinued Application: 87666

Drug Name

SULFINPYRAZONE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-09-17

87666 / 1

Active Ingredient

SULFINPYRAZONE

Application Number

87666

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-09-17

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84031

Drug Name

SULFISOXAZOLE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

84031 / 1

Active Ingredient

SULFISOXAZOLE

Application Number

84031

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
14 Jan
Discontinued Application: 70162

Drug Name

TOLAZAMIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1986-01-14

70162 / 1

Active Ingredient

TOLAZAMIDE

Application Number

70162

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1986-01-14

Regulatory Status

Discontinued

1986
14 Jan
Discontinued Application: 70163

Drug Name

TOLAZAMIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-01-14

70163 / 1

Active Ingredient

TOLAZAMIDE

Application Number

70163

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-01-14

Regulatory Status

Discontinued

1986
14 Jan
Discontinued Application: 70164

Drug Name

TOLAZAMIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-01-14

70164 / 1

Active Ingredient

TOLAZAMIDE

Application Number

70164

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-01-14

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87121

Drug Name

TOLBUTAMIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

87121 / 1

Active Ingredient

TOLBUTAMIDE

Application Number

87121

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2009
27 Mar
Discontinued Application: 76315

Drug Name

TOPIRAMATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2009-03-27

76315 / 1

Active Ingredient

TOPIRAMATE

Application Number

76315

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2009-03-27

Regulatory Status

Discontinued

2009
27 Mar
Discontinued Application: 76315

Drug Name

TOPIRAMATE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2009-03-27

76315 / 2

Active Ingredient

TOPIRAMATE

Application Number

76315

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2009-03-27

Regulatory Status

Discontinued

2009
27 Mar
Discontinued Application: 76315

Drug Name

TOPIRAMATE

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2009-03-27

76315 / 3

Active Ingredient

TOPIRAMATE

Application Number

76315

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2009-03-27

Regulatory Status

Discontinued

2009
15 Apr
Discontinued Application: 76448

Drug Name

TOPIRAMATE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2009-04-15

76448 / 1

Active Ingredient

TOPIRAMATE

Application Number

76448

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2009-04-15

Regulatory Status

Discontinued

2009
15 Apr
Discontinued Application: 76448

Drug Name

TOPIRAMATE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2009-04-15

76448 / 2

Active Ingredient

TOPIRAMATE

Application Number

76448

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2009-04-15

Regulatory Status

Discontinued

2007
22 Jun
Discontinued Application: 77684

Drug Name

TRETINOIN

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2007-06-22

77684 / 1

Active Ingredient

TRETINOIN

Application Number

77684

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2007-06-22

Regulatory Status

Discontinued

2007
26 Oct
Discontinued Application: 76405

Drug Name

TRI-LEGEST 21

Product Number

1

Dosage Form

-

Strength

0.02MG,0.03MG,0.035MG;1MG,1MG,1MG

Approval Date

2007-10-26

76405 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

76405

Product Number

1

Dosage Form

-

Strength

0.02MG,0.03MG,0.035MG;1MG,1MG,1MG

Approval Date

2007-10-26

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84267

Drug Name

TRIAMCINOLONE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

84267 / 1

Active Ingredient

TRIAMCINOLONE

Application Number

84267

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84268

Drug Name

TRIAMCINOLONE

Product Number

1

Dosage Form

-

Strength

8MG

Approval Date

1982-01-01

84268 / 1

Active Ingredient

TRIAMCINOLONE

Application Number

84268

Product Number

1

Dosage Form

-

Strength

8MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84286

Drug Name

TRIAMCINOLONE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

84286 / 1

Active Ingredient

TRIAMCINOLONE

Application Number

84286

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84318

Drug Name

TRIAMCINOLONE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

84318 / 1

Active Ingredient

TRIAMCINOLONE

Application Number

84318

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84319

Drug Name

TRIAMCINOLONE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

84319 / 1

Active Ingredient

TRIAMCINOLONE

Application Number

84319

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84320

Drug Name

TRIAMCINOLONE

Product Number

1

Dosage Form

-

Strength

8MG

Approval Date

1982-01-01

84320 / 1

Active Ingredient

TRIAMCINOLONE

Application Number

84320

Product Number

1

Dosage Form

-

Strength

8MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80744

Drug Name

TRIPELENNAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

80744 / 1

Active Ingredient

TRIPELENNAMINE HYDROCHLORIDE

Application Number

80744

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1997
26 Mar
Discontinued Application: 40145

Drug Name

WARFARIN SODIUM

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1997-03-26

40145 / 1

Active Ingredient

WARFARIN SODIUM

Application Number

40145

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1997-03-26

Regulatory Status

Discontinued

1997
26 Mar
Discontinued Application: 40145

Drug Name

WARFARIN SODIUM

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

1997-03-26

40145 / 2

Active Ingredient

WARFARIN SODIUM

Application Number

40145

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

1997-03-26

Regulatory Status

Discontinued

1997
26 Mar
Discontinued Application: 40145

Drug Name

WARFARIN SODIUM

Product Number

3

Dosage Form

-

Strength

2.5MG

Approval Date

1997-03-26

40145 / 3

Active Ingredient

WARFARIN SODIUM

Application Number

40145

Product Number

3

Dosage Form

-

Strength

2.5MG

Approval Date

1997-03-26

Regulatory Status

Discontinued

1997
26 Mar
Discontinued Application: 40145

Drug Name

WARFARIN SODIUM

Product Number

4

Dosage Form

-

Strength

4MG

Approval Date

1997-03-26

40145 / 4

Active Ingredient

WARFARIN SODIUM

Application Number

40145

Product Number

4

Dosage Form

-

Strength

4MG

Approval Date

1997-03-26

Regulatory Status

Discontinued

1997
26 Mar
Discontinued Application: 40145

Drug Name

WARFARIN SODIUM

Product Number

5

Dosage Form

-

Strength

5MG

Approval Date

1997-03-26

40145 / 5

Active Ingredient

WARFARIN SODIUM

Application Number

40145

Product Number

5

Dosage Form

-

Strength

5MG

Approval Date

1997-03-26

Regulatory Status

Discontinued

1997
26 Mar
Discontinued Application: 40145

Drug Name

WARFARIN SODIUM

Product Number

6

Dosage Form

-

Strength

7.5MG

Approval Date

1997-03-26

40145 / 6

Active Ingredient

WARFARIN SODIUM

Application Number

40145

Product Number

6

Dosage Form

-

Strength

7.5MG

Approval Date

1997-03-26

Regulatory Status

Discontinued

1997
26 Mar
Discontinued Application: 40145

Drug Name

WARFARIN SODIUM

Product Number

7

Dosage Form

-

Strength

10MG

Approval Date

1997-03-26

40145 / 7

Active Ingredient

WARFARIN SODIUM

Application Number

40145

Product Number

7

Dosage Form

-

Strength

10MG

Approval Date

1997-03-26

Regulatory Status

Discontinued

1998
05 Nov
Discontinued Application: 40145

Drug Name

WARFARIN SODIUM

Product Number

8

Dosage Form

-

Strength

3MG

Approval Date

1998-11-05

40145 / 8

Active Ingredient

WARFARIN SODIUM

Application Number

40145

Product Number

8

Dosage Form

-

Strength

3MG

Approval Date

1998-11-05

Regulatory Status

Discontinued

1998
05 Nov
Discontinued Application: 40145

Drug Name

WARFARIN SODIUM

Product Number

9

Dosage Form

-

Strength

6MG

Approval Date

1998-11-05

40145 / 9

Active Ingredient

WARFARIN SODIUM

Application Number

40145

Product Number

9

Dosage Form

-

Strength

6MG

Approval Date

1998-11-05

Regulatory Status

Discontinued

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Drug Status Breakdown
165 total
  • Discontinued
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

ACAMPROSATE CALCIUM

Application Number

200143

Product Number

1

Active Ingredient

ACAMPROSATE CALCIUM

Dosage Form

-

Strength

333MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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