Barr Laboratories Inc.

2013

18 Nov

Discontinued Application: 200143

Drug Name

ACAMPROSATE CALCIUM

Product Number

1

Dosage Form

-

Strength

333MG

Approval Date

2013-11-18

200143 / 1 View Details

Active Ingredient

ACAMPROSATE CALCIUM

Application Number

200143

Product Number

1

Dosage Form

-

Strength

333MG

Approval Date

2013-11-18

Regulatory Status

Discontinued

2013

04 Apr

RX Application: 91455

Drug Name

ACITRETIN

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2013-04-04

91455 / 1 View Details

Active Ingredient

ACITRETIN

Application Number

91455

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2013-04-04

Regulatory Status

RX

2013

04 Apr

RX Application: 91455

Drug Name

ACITRETIN

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2013-04-04

91455 / 2 View Details

Active Ingredient

ACITRETIN

Application Number

91455

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2013-04-04

Regulatory Status

RX

1988

10 May

RX Application: 71111

Drug Name

AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG ANHYDROUS;50MG

Approval Date

1988-05-10

71111 / 1 View Details

Active Ingredient

AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Application Number

71111

Product Number

1

Dosage Form

-

Strength

EQ 5MG ANHYDROUS;50MG

Approval Date

1988-05-10

Regulatory Status

RX

1983

19 Aug

Discontinued Application: 88297

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-08-19

88297 / 1 View Details

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 View Details

Active Ingredient

AMINOPHYLLINE

Application Number

88298

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1983-08-19

Regulatory Status

Discontinued

2004

29 Sep

RX Application: 76783

Drug Name

ARANELLE

Product Number

1

Dosage Form

-

Strength

0.035MG,0.035MG,0.035MG;0.5MG,1MG,0.5MG

Approval Date

2004-09-29

76783 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

76783

Product Number

1

Dosage Form

-

Strength

0.035MG,0.035MG,0.035MG;0.5MG,1MG,0.5MG

Approval Date

2004-09-29

Regulatory Status

RX

-

Unclassified Application: 78612

Drug Name

ARIPIPRAZOLE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

-

78612 / 1 View Details

Active Ingredient

ARIPIPRAZOLE

Application Number

78612

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 78612

Drug Name

ARIPIPRAZOLE

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

-

78612 / 2 View Details

Active Ingredient

ARIPIPRAZOLE

Application Number

78612

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 78612

Drug Name

ARIPIPRAZOLE

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

-

78612 / 3 View Details

Active Ingredient

ARIPIPRAZOLE

Application Number

78612

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 78612

Drug Name

ARIPIPRAZOLE

Product Number

4

Dosage Form

-

Strength

30MG

Approval Date

-

78612 / 4 View Details

Active Ingredient

ARIPIPRAZOLE

Application Number

78612

Product Number

4

Dosage Form

-

Strength

30MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

-

78613 / 1 View Details

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

-

78613 / 2 View Details

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

-

78613 / 3 View Details

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

4

Dosage Form

-

Strength

15MG

Approval Date

-

78613 / 4 View Details

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

4

Dosage Form

-

Strength

15MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

5

Dosage Form

-

Strength

20MG

Approval Date

-

78613 / 5 View Details

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

5

Dosage Form

-

Strength

20MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

6

Dosage Form

-

Strength

30MG

Approval Date

-

78613 / 6 View Details

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

6

Dosage Form

-

Strength

30MG

Approval Date

-

Regulatory Status

Unclassified

2009

14 Aug

RX Application: 78804

Drug Name

ASPIRIN AND DIPYRIDAMOLE

Product Number

1

Dosage Form

-

Strength

25MG;200MG

Approval Date

2009-08-14

78804 / 1 View Details

Active Ingredient

ASPIRIN; DIPYRIDAMOLE

Application Number

78804

Product Number

1

Dosage Form

-

Strength

25MG;200MG

Approval Date

2009-08-14

Regulatory Status

RX

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 View Details

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

2004

22 Apr

RX Application: 76238

Drug Name

BALZIVA-28

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG

Approval Date

2004-04-22

76238 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

76238

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG

Approval Date

2004-04-22

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 84468

Drug Name

BROMPHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

84468 / 1 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

Active Ingredient

CEPHRADINE

Application Number

62859

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

1988-05-19

Regulatory Status

Discontinued

1982

01 Jan

RX Application: 83116

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

83116 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

83116

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 84768

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

84768 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

84768

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 84769

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

84769 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

84769

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

RX

1985

19 Sep

Discontinued Application: 88902

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-09-19

88902 / 1 View Details

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 View Details

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 View Details

Active Ingredient

CHLORZOXAZONE

Application Number

89895

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1988-05-04

Regulatory Status

Discontinued

-

Unclassified Application: 90476

Drug Name

CINACALCET HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

-

90476 / 1 View Details

Active Ingredient

CINACALCET HYDROCHLORIDE

Application Number

90476

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 90476

Drug Name

CINACALCET HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

-

90476 / 2 View Details

Active Ingredient

CINACALCET HYDROCHLORIDE

Application Number

90476

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 90476

Drug Name

CINACALCET HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

90MG

Approval Date

-

90476 / 3 View Details

Active Ingredient

CINACALCET HYDROCHLORIDE

Application Number

90476

Product Number

3

Dosage Form

-

Strength

90MG

Approval Date

-

Regulatory Status

Unclassified

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 View Details

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 View Details

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 View Details

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

74124

Product Number

3

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

Regulatory Status

Discontinued

2005

10 Aug

RX Application: 77194

Drug Name

CLONAZEPAM

Product Number

1

Dosage Form

-

Strength

0.125MG

Approval Date

2005-08-10

77194 / 1 View Details

Active Ingredient

CLONAZEPAM

Application Number

77194

Product Number

1

Dosage Form

-

Strength

0.125MG

Approval Date

2005-08-10

Regulatory Status

RX

2005

10 Aug

RX Application: 77194

Drug Name

CLONAZEPAM

Product Number

2

Dosage Form

-

Strength

0.25MG

Approval Date

2005-08-10

77194 / 2 View Details

Active Ingredient

CLONAZEPAM

Application Number

77194

Product Number

2

Dosage Form

-

Strength

0.25MG

Approval Date

2005-08-10

Regulatory Status

RX

2005

10 Aug

RX Application: 77194

Drug Name

CLONAZEPAM

Product Number

3

Dosage Form

-

Strength

0.5MG

Approval Date

2005-08-10

77194 / 3 View Details

Active Ingredient

CLONAZEPAM

Application Number

77194

Product Number

3

Dosage Form

-

Strength

0.5MG

Approval Date

2005-08-10

Regulatory Status

RX

2005

10 Aug

RX Application: 77194

Drug Name

CLONAZEPAM

Product Number

4

Dosage Form

-

Strength

1MG

Approval Date

2005-08-10

77194 / 4 View Details

Active Ingredient

CLONAZEPAM

Application Number

77194

Product Number

4

Dosage Form

-

Strength

1MG

Approval Date

2005-08-10

Regulatory Status

RX

2005

10 Aug

RX Application: 77194

Drug Name

CLONAZEPAM

Product Number

5

Dosage Form

-

Strength

2MG

Approval Date

2005-08-10

77194 / 5 View Details

Active Ingredient

CLONAZEPAM

Application Number

77194

Product Number

5

Dosage Form

-

Strength

2MG

Approval Date

2005-08-10

Regulatory Status

RX

2015

25 Nov

RX Application: 90308

Drug Name

CLOZAPINE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2015-11-25

90308 / 1 View Details

Active Ingredient

CLOZAPINE

Application Number

90308

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2015-11-25

Regulatory Status

RX

2015

25 Nov

RX Application: 90308

Drug Name

CLOZAPINE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2015-11-25

90308 / 2 View Details

Active Ingredient

CLOZAPINE

Application Number

90308

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2015-11-25

Regulatory Status

RX

2018

09 Apr

RX Application: 90308

Drug Name

CLOZAPINE

Product Number

3

Dosage Form

-

Strength

12.5MG

Approval Date

2018-04-09

90308 / 3 View Details

Active Ingredient

CLOZAPINE

Application Number

90308

Product Number

3

Dosage Form

-

Strength

12.5MG

Approval Date

2018-04-09

Regulatory Status

RX

2015

25 Nov

RX Application: 90308

Drug Name

CLOZAPINE

Product Number

4

Dosage Form

-

Strength

150MG

Approval Date

2015-11-25

90308 / 4 View Details

Active Ingredient

CLOZAPINE

Application Number

90308

Product Number

4

Dosage Form

-

Strength

150MG

Approval Date

2015-11-25

Regulatory Status

RX

2015

25 Nov

RX Application: 90308

Drug Name

CLOZAPINE

Product Number

5

Dosage Form

-

Strength

200MG

Approval Date

2015-11-25

90308 / 5 View Details

Active Ingredient

CLOZAPINE

Application Number

90308

Product Number

5

Dosage Form

-

Strength

200MG

Approval Date

2015-11-25

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 83471

Drug Name

CORTISONE ACETATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

83471 / 1 View Details

Active Ingredient

CORTISONE ACETATE

Application Number

83471

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1996

09 Aug

RX Application: 74582

Drug Name

DANAZOL

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1996-08-09

74582 / 1 View Details

Active Ingredient

DANAZOL

Application Number

74582

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1996-08-09

Regulatory Status

RX

1998

29 May

RX Application: 74582

Drug Name

DANAZOL

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1998-05-29

74582 / 2 View Details

Active Ingredient

DANAZOL

Application Number

74582

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1998-05-29

Regulatory Status

RX

1998

29 May

RX Application: 74582

Drug Name

DANAZOL

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1998-05-29

74582 / 3 View Details

Active Ingredient

DANAZOL

Application Number

74582

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1998-05-29

Regulatory Status

RX

2004

13 Dec

Discontinued Application: 65171

Drug Name

DEMECLOCYCLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2004-12-13

65171 / 1 View Details

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 View Details

Active Ingredient

DEMECLOCYCLINE HYDROCHLORIDE

Application Number

65171

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2004-12-13

Regulatory Status

Discontinued

2002

11 Feb

RX Application: 40422

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

2002-02-11

40422 / 1 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

40422

Product Number

1

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG

Approval Date

2002-02-11

Regulatory Status

RX

2002

11 Feb

RX Application: 40422

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

2002-02-11

40422 / 2 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

40422

Product Number

2

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG

Approval Date

2002-02-11

Regulatory Status

RX

2002

11 Feb

RX Application: 40422

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

3

Dosage Form

-

Strength

5MG;5MG;5MG;5MG

Approval Date

2002-02-11

40422 / 3 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

40422

Product Number

3

Dosage Form

-

Strength

5MG;5MG;5MG;5MG

Approval Date

2002-02-11

Regulatory Status

RX

2002

11 Feb

RX Application: 40422

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

4

Dosage Form

-

Strength

7.5MG;7.5MG;7.5MG;7.5MG

Approval Date

2002-02-11

40422 / 4 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

40422

Product Number

4

Dosage Form

-

Strength

7.5MG;7.5MG;7.5MG;7.5MG

Approval Date

2002-02-11

Regulatory Status

RX

2003

19 Mar

RX Application: 40422

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

5

Dosage Form

-

Strength

1.875MG;1.875MG;1.875MG;1.875MG

Approval Date

2003-03-19

40422 / 5 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

40422

Product Number

5

Dosage Form

-

Strength

1.875MG;1.875MG;1.875MG;1.875MG

Approval Date

2003-03-19

Regulatory Status

RX

2003

19 Mar

RX Application: 40422

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

6

Dosage Form

-

Strength

3.125MG;3.125MG;3.125MG;3.125MG

Approval Date

2003-03-19

40422 / 6 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

40422

Product Number

6

Dosage Form

-

Strength

3.125MG;3.125MG;3.125MG;3.125MG

Approval Date

2003-03-19

Regulatory Status

RX

2003

19 Mar

RX Application: 40422

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

7

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG

Approval Date

2003-03-19

40422 / 7 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

40422

Product Number

7

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG

Approval Date

2003-03-19

Regulatory Status

RX

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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

2001

31 Jan

RX Application: 40361

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2001-01-31

40361 / 1 View Details

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

40361

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2001-01-31

Regulatory Status

RX

2001

31 Jan

RX Application: 40361

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2001-01-31

40361 / 2 View Details

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

40361

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2001-01-31

Regulatory Status

RX

1985

01 Nov

Discontinued Application: 70152

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1985-11-01

70152 / 1 View Details

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 View Details

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 View Details

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 View Details

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 View Details

Active Ingredient

DIDANOSINE

Application Number

77167

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2004-12-03

Regulatory Status

Discontinued

1990

03 Oct

RX Application: 87184

Drug Name

DIPYRIDAMOLE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1990-10-03

87184 / 1 View Details

Active Ingredient

DIPYRIDAMOLE

Application Number

87184

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1990-10-03

Regulatory Status

RX

1990

03 Oct

RX Application: 87716

Drug Name

DIPYRIDAMOLE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1990-10-03

87716 / 1 View Details

Active Ingredient

DIPYRIDAMOLE

Application Number

87716

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1990-10-03

Regulatory Status

RX

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 View Details

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 View Details

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

2010

21 Dec

RX Application: 90095

Drug Name

DUTASTERIDE

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2010-12-21

90095 / 1 View Details

Active Ingredient

DUTASTERIDE

Application Number

90095

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2010-12-21

Regulatory Status

RX

1988

25 Nov

Discontinued Application: 62999

Drug Name

E-BASE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1988-11-25

62999 / 1 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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

1997

22 Oct

RX Application: 40197

Drug Name

ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1997-10-22

40197 / 1 View Details

Active Ingredient

ESTRADIOL

Application Number

40197

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1997-10-22

Regulatory Status

RX

1997

22 Oct

RX Application: 40197

Drug Name

ESTRADIOL

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

1997-10-22

40197 / 2 View Details

Active Ingredient

ESTRADIOL

Application Number

40197

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

1997-10-22

Regulatory Status

RX

1997

22 Oct

RX Application: 40197

Drug Name

ESTRADIOL

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

1997-10-22

40197 / 3 View Details

Active Ingredient

ESTRADIOL

Application Number

40197

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

1997-10-22

Regulatory Status

RX

2010

11 May

RX Application: 79193

Drug Name

ESTRADIOL AND NORETHINDRONE ACETATE

Product Number

1

Dosage Form

-

Strength

1MG;0.5MG

Approval Date

2010-05-11

79193 / 1 View Details

Active Ingredient

ESTRADIOL; NORETHINDRONE ACETATE

Application Number

79193

Product Number

1

Dosage Form

-

Strength

1MG;0.5MG

Approval Date

2010-05-11

Regulatory Status

RX

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

Active Ingredient

FOLIC ACID

Application Number

89177

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1986-01-08

Regulatory Status

Discontinued

2008

28 Aug

RX Application: 77605

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2008-08-28

77605 / 1 View Details

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

77605

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2008-08-28

Regulatory Status

RX

2008

28 Aug

RX Application: 77605

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2008-08-28

77605 / 2 View Details

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

77605

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2008-08-28

Regulatory Status

RX

2008

28 Aug

RX Application: 77605

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

3

Dosage Form

-

Strength

EQ 12MG BASE

Approval Date

2008-08-28

77605 / 3 View Details

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

77605

Product Number

3

Dosage Form

-

Strength

EQ 12MG BASE

Approval Date

2008-08-28

Regulatory Status

RX

2008

15 Sep

RX Application: 78189

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2008-09-15

78189 / 1 View Details

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

78189

Product Number

1

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2008-09-15

Regulatory Status

RX

2008

15 Sep

RX Application: 78189

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

2

Dosage Form

-

Strength

EQ 16MG BASE

Approval Date

2008-09-15

78189 / 2 View Details

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

78189

Product Number

2

Dosage Form

-

Strength

EQ 16MG BASE

Approval Date

2008-09-15

Regulatory Status

RX

2008

15 Sep

RX Application: 78189

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

3

Dosage Form

-

Strength

EQ 24MG BASE

Approval Date

2008-09-15

78189 / 3 View Details

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

78189

Product Number

3

Dosage Form

-

Strength

EQ 24MG BASE

Approval Date

2008-09-15

Regulatory Status

RX

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

Active Ingredient

HYDROXYUREA

Application Number

75020

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

2000-06-26

Regulatory Status

Discontinued

1998

16 Oct

RX Application: 75143

Drug Name

HYDROXYUREA

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1998-10-16

75143 / 1 View Details

Active Ingredient

HYDROXYUREA

Application Number

75143

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1998-10-16

Regulatory Status

RX

2000

21 Sep

Discontinued Application: 75143

Drug Name

HYDROXYUREA

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

2000-09-21

75143 / 2 View Details

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 View Details

Active Ingredient

HYDROXYUREA

Application Number

75734

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

2000-08-29

Regulatory Status

Discontinued

1984

15 Jun

RX Application: 88496

Drug Name

HYDROXYZINE PAMOATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1984-06-15

88496 / 1 View Details

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

88496

Product Number

1

Dosage Form

-

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1984-06-15

Regulatory Status

RX

2003

30 May

RX Application: 76381

Drug Name

JUNEL 1.5/30

Product Number

1

Dosage Form

-

Strength

0.03MG;1.5MG

Approval Date

2003-05-30

76381 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

76381

Product Number

1

Dosage Form

-

Strength

0.03MG;1.5MG

Approval Date

2003-05-30

Regulatory Status

RX

2003

18 Sep

RX Application: 76064

Drug Name

JUNEL FE 1.5/30

Product Number

1

Dosage Form

-

Strength

0.03MG;1.5MG

Approval Date

2003-09-18

76064 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

76064

Product Number

1

Dosage Form

-

Strength

0.03MG;1.5MG

Approval Date

2003-09-18

Regulatory Status

RX

2003

18 Sep

RX Application: 76081

Drug Name

JUNEL FE 1/20

Product Number

1

Dosage Form

-

Strength

0.02MG;1MG

Approval Date

2003-09-18

76081 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

76081

Product Number

1

Dosage Form

-

Strength

0.02MG;1MG

Approval Date

2003-09-18

Regulatory Status

RX

2002

05 Apr

RX Application: 75863

Drug Name

KARIVA

Product Number

1

Dosage Form

-

Strength

0.15MG,N/A;0.02MG,0.01MG

Approval Date

2002-04-05

75863 / 1 View Details

Active Ingredient

DESOGESTREL; ETHINYL ESTRADIOL

Application Number

75863

Product Number

1

Dosage Form

-

Strength

0.15MG,N/A;0.02MG,0.01MG

Approval Date

2002-04-05

Regulatory Status

RX

2005

23 May

RX Application: 76785

Drug Name

KELNOR

Product Number

1

Dosage Form

-

Strength

0.035MG;1MG

Approval Date

2005-05-23

76785 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE

Application Number

76785

Product Number

1

Dosage Form

-

Strength

0.035MG;1MG

Approval Date

2005-05-23

Regulatory Status

RX

2022

27 Jan

RX Application: 90977

Drug Name

LANTHANUM CARBONATE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2022-01-27

90977 / 1 View Details

Active Ingredient

LANTHANUM CARBONATE

Application Number

90977

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2022-01-27

Regulatory Status

RX

2022

27 Jan

RX Application: 90977

Drug Name

LANTHANUM CARBONATE

Product Number

2

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2022-01-27

90977 / 2 View Details

Active Ingredient

LANTHANUM CARBONATE

Application Number

90977

Product Number

2

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2022-01-27

Regulatory Status

RX

2022

27 Jan

RX Application: 90977

Drug Name

LANTHANUM CARBONATE

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

2022-01-27

90977 / 3 View Details

Active Ingredient

LANTHANUM CARBONATE

Application Number

90977

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

2022-01-27

Regulatory Status

RX

2005

13 Sep

Discontinued Application: 77083

Drug Name

LEFLUNOMIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2005-09-13

77083 / 1 View Details

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 View Details

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 View Details

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

2002

20 Mar

RX Application: 75803

Drug Name

LESSINA-28

Product Number

2

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2002-03-20

75803 / 2 View Details

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

75803

Product Number

2

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2002-03-20

Regulatory Status

RX

1987

24 Sep

RX Application: 71198

Drug Name

LEUCOVORIN CALCIUM

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1987-09-24

71198 / 1 View Details

Active Ingredient

LEUCOVORIN CALCIUM

Application Number

71198

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1987-09-24

Regulatory Status

RX

1987

24 Sep

RX Application: 71199

Drug Name

LEUCOVORIN CALCIUM

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1987-09-24

71199 / 1 View Details

Active Ingredient

LEUCOVORIN CALCIUM

Application Number

71199

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1987-09-24

Regulatory Status

RX

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 View Details

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 View Details

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 View Details

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 View Details

Active Ingredient

MECLOFENAMATE SODIUM

Application Number

72848

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1989-03-20

Regulatory Status

Discontinued

1996

09 Aug

RX Application: 40159

Drug Name

MEDROXYPROGESTERONE ACETATE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1996-08-09

40159 / 1 View Details

Active Ingredient

MEDROXYPROGESTERONE ACETATE

Application Number

40159

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1996-08-09

Regulatory Status

RX

1996

09 Aug

RX Application: 40159

Drug Name

MEDROXYPROGESTERONE ACETATE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1996-08-09

40159 / 2 View Details

Active Ingredient

MEDROXYPROGESTERONE ACETATE

Application Number

40159

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1996-08-09

Regulatory Status

RX

1996

09 Aug

RX Application: 40159

Drug Name

MEDROXYPROGESTERONE ACETATE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1996-08-09

40159 / 3 View Details

Active Ingredient

MEDROXYPROGESTERONE ACETATE

Application Number

40159

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1996-08-09

Regulatory Status

RX

2003

29 Dec

RX Application: 76392

Drug Name

MEFLOQUINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2003-12-29

76392 / 1 View Details

Active Ingredient

MEFLOQUINE HYDROCHLORIDE

Application Number

76392

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2003-12-29

Regulatory Status

RX

1995

30 Nov

RX Application: 74621

Drug Name

MEGESTROL ACETATE

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1995-11-30

74621 / 1 View Details

Active Ingredient

MEGESTROL ACETATE

Application Number

74621

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1995-11-30

Regulatory Status

RX

1996

16 Aug

RX Application: 74621

Drug Name

MEGESTROL ACETATE

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

1996-08-16

74621 / 2 View Details

Active Ingredient

MEGESTROL ACETATE

Application Number

74621

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

1996-08-16

Regulatory Status

RX

1984

02 Jul

Discontinued Application: 88639

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1984-07-02

88639 / 1 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

76863

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

2004-10-14

Regulatory Status

Discontinued

1990

15 Oct

RX Application: 81099

Drug Name

METHOTREXATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

1990-10-15

81099 / 1 View Details

Active Ingredient

METHOTREXATE SODIUM

Application Number

81099

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

1990-10-15

Regulatory Status

RX

2012

13 Jul

Discontinued Application: 79031

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2012-07-13

79031 / 1 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

Active Ingredient

MINOCYCLINE HYDROCHLORIDE

Application Number

65485

Product Number

8

Dosage Form

-

Strength

EQ 105MG BASE

Approval Date

2017-04-26

Regulatory Status

Discontinued

-

Unclassified Application: 76597

Drug Name

MODAFINIL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

76597 / 1 View Details

Active Ingredient

MODAFINIL

Application Number

76597

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 76597

Drug Name

MODAFINIL

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

-

76597 / 2 View Details

Active Ingredient

MODAFINIL

Application Number

76597

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

-

Regulatory Status

Unclassified

1998

08 May

RX Application: 74918

Drug Name

NALTREXONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1998-05-08

74918 / 1 View Details

Active Ingredient

NALTREXONE HYDROCHLORIDE

Application Number

74918

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1998-05-08

Regulatory Status

RX

2005

14 Apr

RX Application: 76250

Drug Name

NIACIN

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

2005-04-14

76250 / 1 View Details

Active Ingredient

NIACIN

Application Number

76250

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

2005-04-14

Regulatory Status

RX

2005

26 Apr

RX Application: 76378

Drug Name

NIACIN

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2005-04-26

76378 / 1 View Details

Active Ingredient

NIACIN

Application Number

76378

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2005-04-26

Regulatory Status

RX

2005

26 Apr

RX Application: 76378

Drug Name

NIACIN

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2005-04-26

76378 / 2 View Details

Active Ingredient

NIACIN

Application Number

76378

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2005-04-26

Regulatory Status

RX

2001

25 May

RX Application: 75951

Drug Name

NORETHINDRONE ACETATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2001-05-25

75951 / 1 View Details

Active Ingredient

NORETHINDRONE ACETATE

Application Number

75951

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2001-05-25

Regulatory Status

RX

2009

06 Nov

RX Application: 76221

Drug Name

NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.005MG;1MG

Approval Date

2009-11-06

76221 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

76221

Product Number

1

Dosage Form

-

Strength

0.005MG;1MG

Approval Date

2009-11-06

Regulatory Status

RX

2010

05 Aug

RX Application: 78965

Drug Name

NORETHINDRONE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG

Approval Date

2010-08-05

78965 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

78965

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG

Approval Date

2010-08-05

Regulatory Status

RX

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 View Details

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

1992

28 Feb

RX Application: 72693

Drug Name

NORTREL 1/35-21

Product Number

1

Dosage Form

-

Strength

0.035MG;1MG

Approval Date

1992-02-28

72693 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

72693

Product Number

1

Dosage Form

-

Strength

0.035MG;1MG

Approval Date

1992-02-28

Regulatory Status

RX

2002

30 Aug

RX Application: 75478

Drug Name

NORTREL 7/7/7

Product Number

1

Dosage Form

-

Strength

0.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG

Approval Date

2002-08-30

75478 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

75478

Product Number

1

Dosage Form

-

Strength

0.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG

Approval Date

2002-08-30

Regulatory Status

RX

2002

30 Aug

RX Application: 75478

Drug Name

NORTREL 7/7/7

Product Number

2

Dosage Form

-

Strength

0.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG

Approval Date

2002-08-30

75478 / 2 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

75478

Product Number

2

Dosage Form

-

Strength

0.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG

Approval Date

2002-08-30

Regulatory Status

RX

2012

30 Jan

RX Application: 77243

Drug Name

OLANZAPINE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2012-01-30

77243 / 1 View Details

Active Ingredient

OLANZAPINE

Application Number

77243

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2012-01-30

Regulatory Status

RX

2012

30 Jan

RX Application: 77243

Drug Name

OLANZAPINE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2012-01-30

77243 / 2 View Details

Active Ingredient

OLANZAPINE

Application Number

77243

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2012-01-30

Regulatory Status

RX

2012

30 Jan

RX Application: 77243

Drug Name

OLANZAPINE

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2012-01-30

77243 / 3 View Details

Active Ingredient

OLANZAPINE

Application Number

77243

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2012-01-30

Regulatory Status

RX

2012

30 Jan

RX Application: 77243

Drug Name

OLANZAPINE

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2012-01-30

77243 / 4 View Details

Active Ingredient

OLANZAPINE

Application Number

77243

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2012-01-30

Regulatory Status

RX

2015

13 Jul

OTC Application: 90848

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2015-07-13

90848 / 1 View Details

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

90848

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2015-07-13

Regulatory Status

OTC

2007

25 Jun

Discontinued Application: 76693

Drug Name

ONDANSETRON

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2007-06-25

76693 / 1 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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

2002

23 May

RX Application: 75866

Drug Name

PORTIA-28

Product Number

2

Dosage Form

-

Strength

0.03MG;0.15MG

Approval Date

2002-05-23

75866 / 2 View Details

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

75866

Product Number

2

Dosage Form

-

Strength

0.03MG;0.15MG

Approval Date

2002-05-23

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 84426

Drug Name

PREDNISOLONE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

84426 / 2 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

Active Ingredient

SECOBARBITAL SODIUM

Application Number

84225

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2002

25 Sep

RX Application: 75804

Drug Name

SPRINTEC

Product Number

1

Dosage Form

-

Strength

0.035MG;0.25MG

Approval Date

2002-09-25

75804 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORGESTIMATE

Application Number

75804

Product Number

1

Dosage Form

-

Strength

0.035MG;0.25MG

Approval Date

2002-09-25

Regulatory Status

RX

1983

25 Jul

Discontinued Application: 87189

Drug Name

SULFAMETHOXAZOLE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1983-07-25

87189 / 1 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

Active Ingredient

TRETINOIN

Application Number

77684

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2007-06-22

Regulatory Status

Discontinued

2001

21 Mar

RX Application: 40385

Drug Name

TREXALL

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2001-03-21

40385 / 1 View Details

Active Ingredient

METHOTREXATE SODIUM

Application Number

40385

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2001-03-21

Regulatory Status

RX

2001

21 Mar

RX Application: 40385

Drug Name

TREXALL

Product Number

2

Dosage Form

-

Strength

EQ 7.5MG BASE

Approval Date

2001-03-21

40385 / 2 View Details

Active Ingredient

METHOTREXATE SODIUM

Application Number

40385

Product Number

2

Dosage Form

-

Strength

EQ 7.5MG BASE

Approval Date

2001-03-21

Regulatory Status

RX

2001

21 Mar

RX Application: 40385

Drug Name

TREXALL

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2001-03-21

40385 / 3 View Details

Active Ingredient

METHOTREXATE SODIUM

Application Number

40385

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2001-03-21

Regulatory Status

RX

2001

21 Mar

RX Application: 40385

Drug Name

TREXALL

Product Number

4

Dosage Form

-

Strength

EQ 15MG BASE

Approval Date

2001-03-21

40385 / 4 View Details

Active Ingredient

METHOTREXATE SODIUM

Application Number

40385

Product Number

4

Dosage Form

-

Strength

EQ 15MG BASE

Approval Date

2001-03-21

Regulatory Status

RX

2009

29 Jun

RX Application: 76784

Drug Name

TRI LO SPRINTEC

Product Number

1

Dosage Form

-

Strength

0.025MG,0.025MG,0.025MG;0.18MG,0.215MG,0.25MG

Approval Date

2009-06-29

76784 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORGESTIMATE

Application Number

76784

Product Number

1

Dosage Form

-

Strength

0.025MG,0.025MG,0.025MG;0.18MG,0.215MG,0.25MG

Approval Date

2009-06-29

Regulatory Status

RX

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 View Details

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

2007

26 Oct

RX Application: 76105

Drug Name

TRI-LEGEST FE

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2007-10-26

76105 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

76105

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2007-10-26

Regulatory Status

RX

2003

29 Dec

RX Application: 75808

Drug Name

TRI-SPRINTEC

Product Number

1

Dosage Form

-

Strength

0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG

Approval Date

2003-12-29

75808 / 1 View Details

Active Ingredient

ETHINYL ESTRADIOL; NORGESTIMATE

Application Number

75808

Product Number

1

Dosage Form

-

Strength

0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG

Approval Date

2003-12-29

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 84267

Drug Name

TRIAMCINOLONE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

84267 / 1 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

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 View Details

Active Ingredient

WARFARIN SODIUM

Application Number

40145

Product Number

9

Dosage Form

-

Strength

6MG

Approval Date

1998-11-05

Regulatory Status

Discontinued

-

Unclassified Application: 74047

Drug Name

ZIDOVUDINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

74047 / 1 View Details

Active Ingredient

ZIDOVUDINE

Application Number

74047

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

Barr Laboratories Inc.
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Barr Laboratories Inc. FDA Approved Drugs