Assia Chemical Industries Ltd Discontinued

1983

29 Dec

Discontinued Application: 88324

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1983-12-29

88324 / 1 View Details

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

88324

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1983-12-29

Regulatory Status

Discontinued

1984

04 Jun

Discontinued Application: 88537

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;15MG

Approval Date

1984-06-04

88537 / 1 View Details

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

88537

Product Number

1

Dosage Form

-

Strength

300MG;15MG

Approval Date

1984-06-04

Regulatory Status

Discontinued

1984

01 Jun

Discontinued Application: 88599

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;60MG

Approval Date

1984-06-01

88599 / 1 View Details

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

88599

Product Number

1

Dosage Form

-

Strength

300MG;60MG

Approval Date

1984-06-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86535

Drug Name

ACTICORT

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

86535 / 1 View Details

Active Ingredient

HYDROCORTISONE

Application Number

86535

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1997

22 Apr

Discontinued Application: 74556

Drug Name

ACYCLOVIR

Product Number

1

Dosage Form

-

Strength

200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1997-04-22

74556 / 1 View Details

Active Ingredient

ACYCLOVIR

Application Number

74556

Product Number

1

Dosage Form

-

Strength

200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1997-04-22

Regulatory Status

Discontinued

1997

22 Apr

Discontinued Application: 74828

Drug Name

ACYCLOVIR

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1997-04-22

74828 / 1 View Details

Active Ingredient

ACYCLOVIR

Application Number

74828

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1997-04-22

Regulatory Status

Discontinued

1983

02 Aug

Discontinued Application: 88023

Drug Name

ADIPEX-P

Product Number

1

Dosage Form

-

Strength

37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-08-02

88023 / 1 View Details

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

88023

Product Number

1

Dosage Form

-

Strength

37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-08-02

Regulatory Status

Discontinued

1989

05 Dec

Discontinued Application: 72619

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1989-12-05

72619 / 1 View Details

Active Ingredient

ALBUTEROL SULFATE

Application Number

72619

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1989-12-05

Regulatory Status

Discontinued

1989

05 Dec

Discontinued Application: 72620

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

1989-12-05

72620 / 1 View Details

Active Ingredient

ALBUTEROL SULFATE

Application Number

72620

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

1989-12-05

Regulatory Status

Discontinued

1993

25 Jun

Discontinued Application: 72779

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1993-06-25

72779 / 1 View Details

Active Ingredient

ALBUTEROL SULFATE

Application Number

72779

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1993-06-25

Regulatory Status

Discontinued

1993

25 Jun

Discontinued Application: 72780

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

1993-06-25

72780 / 1 View Details

Active Ingredient

ALBUTEROL SULFATE

Application Number

72780

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

1993-06-25

Regulatory Status

Discontinued

1990

30 Mar

Discontinued Application: 72938

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1990-03-30

72938 / 1 View Details

Active Ingredient

ALBUTEROL SULFATE

Application Number

72938

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1990-03-30

Regulatory Status

Discontinued

1990

30 Mar

Discontinued Application: 72939

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

1990-03-30

72939 / 1 View Details

Active Ingredient

ALBUTEROL SULFATE

Application Number

72939

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

1990-03-30

Regulatory Status

Discontinued

1988

17 Apr

Discontinued Application: 70795

Drug Name

AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG ANHYDROUS;50MG

Approval Date

1988-04-17

70795 / 1 View Details

Active Ingredient

AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Application Number

70795

Product Number

1

Dosage Form

-

Strength

EQ 5MG ANHYDROUS;50MG

Approval Date

1988-04-17

Regulatory Status

Discontinued

1999

16 Apr

Discontinued Application: 74895

Drug Name

AMIODARONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1999-04-16

74895 / 1 View Details

Active Ingredient

AMIODARONE HYDROCHLORIDE

Application Number

74895

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1999-04-16

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85836

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

85836 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

85836

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86610

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

86610 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86610

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86853

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

1982-01-01

86853 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86853

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86854

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

86854 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86854

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86857

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

86857 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86857

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86859

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

86859 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86859

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86860

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1982-01-01

86860 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86860

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987

22 Dec

Discontinued Application: 62853

Drug Name

AMOXICILLIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1987-12-22

62853 / 1 View Details

Active Ingredient

AMOXICILLIN

Application Number

62853

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1987-12-22

Regulatory Status

Discontinued

1987

22 Dec

Discontinued Application: 62854

Drug Name

AMOXICILLIN

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1987-12-22

62854 / 1 View Details

Active Ingredient

AMOXICILLIN

Application Number

62854

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1987-12-22

Regulatory Status

Discontinued

1988

01 Nov

Discontinued Application: 62946

Drug Name

AMOXICILLIN

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1988-11-01

62946 / 1 View Details

Active Ingredient

AMOXICILLIN

Application Number

62946

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1988-11-01

Regulatory Status

Discontinued

1989

06 Jan

Discontinued Application: 63001

Drug Name

AMOXICILLIN

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

1989-01-06

63001 / 1 View Details

Active Ingredient

AMOXICILLIN

Application Number

63001

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

1989-01-06

Regulatory Status

Discontinued

1989

28 Feb

Discontinued Application: 63030

Drug Name

AMOXICILLIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1989-02-28

63030 / 1 View Details

Active Ingredient

AMOXICILLIN

Application Number

63030

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1989-02-28

Regulatory Status

Discontinued

1989

28 Feb

Discontinued Application: 63031

Drug Name

AMOXICILLIN

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1989-02-28

63031 / 1 View Details

Active Ingredient

AMOXICILLIN

Application Number

63031

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1989-02-28

Regulatory Status

Discontinued

1996

19 Dec

Discontinued Application: 64031

Drug Name

AMOXICILLIN

Product Number

1

Dosage Form

-

Strength

125MG

Approval Date

1996-12-19

64031 / 1 View Details

Active Ingredient

AMOXICILLIN

Application Number

64031

Product Number

1

Dosage Form

-

Strength

125MG

Approval Date

1996-12-19

Regulatory Status

Discontinued

1996

19 Dec

Discontinued Application: 64031

Drug Name

AMOXICILLIN

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

1996-12-19

64031 / 2 View Details

Active Ingredient

AMOXICILLIN

Application Number

64031

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

1996-12-19

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 61370

Drug Name

AMPICILLIN TRIHYDRATE

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

61370 / 1 View Details

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61370

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 61370

Drug Name

AMPICILLIN TRIHYDRATE

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

61370 / 2 View Details

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61370

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993

28 May

Discontinued Application: 73315

Drug Name

ATENOLOL

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1993-05-28

73315 / 1 View Details

Active Ingredient

ATENOLOL

Application Number

73315

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1993-05-28

Regulatory Status

Discontinued

1993

28 May

Discontinued Application: 73316

Drug Name

ATENOLOL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1993-05-28

73316 / 1 View Details

Active Ingredient

ATENOLOL

Application Number

73316

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1993-05-28

Regulatory Status

Discontinued

2005

14 Nov

Discontinued Application: 65150

Drug Name

AZITHROMYCIN

Product Number

1

Dosage Form

-

Strength

EQ 600MG BASE

Approval Date

2005-11-14

65150 / 1 View Details

Active Ingredient

AZITHROMYCIN

Application Number

65150

Product Number

1

Dosage Form

-

Strength

EQ 600MG BASE

Approval Date

2005-11-14

Regulatory Status

Discontinued

2005

14 Nov

Discontinued Application: 65153

Drug Name

AZITHROMYCIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2005-11-14

65153 / 1 View Details

Active Ingredient

AZITHROMYCIN

Application Number

65153

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2005-11-14

Regulatory Status

Discontinued

1992

27 Feb

Discontinued Application: 73043

Drug Name

BACLOFEN

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1992-02-27

73043 / 1 View Details

Active Ingredient

BACLOFEN

Application Number

73043

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1992-02-27

Regulatory Status

Discontinued

1992

27 Feb

Discontinued Application: 73044

Drug Name

BACLOFEN

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1992-02-27

73044 / 1 View Details

Active Ingredient

BACLOFEN

Application Number

73044

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1992-02-27

Regulatory Status

Discontinued

1987

10 Aug

Discontinued Application: 71476

Drug Name

BETAMETHASONE DIPROPIONATE

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

1987-08-10

71476 / 1 View Details

Active Ingredient

BETAMETHASONE DIPROPIONATE

Application Number

71476

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

1987-08-10

Regulatory Status

Discontinued

1987

10 Aug

Discontinued Application: 71477

Drug Name

BETAMETHASONE DIPROPIONATE

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

1987-08-10

71477 / 1 View Details

Active Ingredient

BETAMETHASONE DIPROPIONATE

Application Number

71477

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

1987-08-10

Regulatory Status

Discontinued

2009

06 Jul

Discontinued Application: 76932

Drug Name

BICALUTAMIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2009-07-06

76932 / 1 View Details

Active Ingredient

BICALUTAMIDE

Application Number

76932

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2009-07-06

Regulatory Status

Discontinued

2001

19 Jan

Discontinued Application: 75686

Drug Name

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

2.5MG;6.25MG

Approval Date

2001-01-19

75686 / 1 View Details

Active Ingredient

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Application Number

75686

Product Number

1

Dosage Form

-

Strength

2.5MG;6.25MG

Approval Date

2001-01-19

Regulatory Status

Discontinued

2001

19 Jan

Discontinued Application: 75686

Drug Name

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

5MG;6.25MG

Approval Date

2001-01-19

75686 / 2 View Details

Active Ingredient

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Application Number

75686

Product Number

2

Dosage Form

-

Strength

5MG;6.25MG

Approval Date

2001-01-19

Regulatory Status

Discontinued

2001

19 Jan

Discontinued Application: 75686

Drug Name

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

10MG;6.25MG

Approval Date

2001-01-19

75686 / 3 View Details

Active Ingredient

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Application Number

75686

Product Number

3

Dosage Form

-

Strength

10MG;6.25MG

Approval Date

2001-01-19

Regulatory Status

Discontinued

1985

01 May

Discontinued Application: 88631

Drug Name

BUTABARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1985-05-01

88631 / 1 View Details

Active Ingredient

BUTABARBITAL SODIUM

Application Number

88631

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1985-05-01

Regulatory Status

Discontinued

1985

18 May

Discontinued Application: 88632

Drug Name

BUTABARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1985-05-18

88632 / 1 View Details

Active Ingredient

BUTABARBITAL SODIUM

Application Number

88632

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1985-05-18

Regulatory Status

Discontinued

1996

13 Feb

Discontinued Application: 74322

Drug Name

CAPTOPRIL

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

1996-02-13

74322 / 1 View Details

Active Ingredient

CAPTOPRIL

Application Number

74322

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

1996-02-13

Regulatory Status

Discontinued

1996

13 Feb

Discontinued Application: 74322

Drug Name

CAPTOPRIL

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1996-02-13

74322 / 2 View Details

Active Ingredient

CAPTOPRIL

Application Number

74322

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1996-02-13

Regulatory Status

Discontinued

1996

13 Feb

Discontinued Application: 74322

Drug Name

CAPTOPRIL

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1996-02-13

74322 / 3 View Details

Active Ingredient

CAPTOPRIL

Application Number

74322

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1996-02-13

Regulatory Status

Discontinued

1996

13 Feb

Discontinued Application: 74322

Drug Name

CAPTOPRIL

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

1996-02-13

74322 / 4 View Details

Active Ingredient

CAPTOPRIL

Application Number

74322

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

1996-02-13

Regulatory Status

Discontinued

1996

16 Sep

Discontinued Application: 64081

Drug Name

CEFACLOR

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1996-09-16

64081 / 1 View Details

Active Ingredient

CEFACLOR

Application Number

64081

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1996-09-16

Regulatory Status

Discontinued

1996

16 Sep

Discontinued Application: 64081

Drug Name

CEFACLOR

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1996-09-16

64081 / 2 View Details

Active Ingredient

CEFACLOR

Application Number

64081

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1996-09-16

Regulatory Status

Discontinued

1996

24 Jun

Discontinued Application: 64145

Drug Name

CEFACLOR

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1996-06-24

64145 / 1 View Details

Active Ingredient

CEFACLOR

Application Number

64145

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1996-06-24

Regulatory Status

Discontinued

1996

24 Jun

Discontinued Application: 64145

Drug Name

CEFACLOR

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1996-06-24

64145 / 2 View Details

Active Ingredient

CEFACLOR

Application Number

64145

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1996-06-24

Regulatory Status

Discontinued

1989

10 Feb

Discontinued Application: 62695

Drug Name

CEFADROXIL

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1989-02-10

62695 / 1 View Details

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

62695

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1989-02-10

Regulatory Status

Discontinued

2006

29 Jun

Discontinued Application: 65262

Drug Name

CEFTRIAXONE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2006-06-29

65262 / 1 View Details

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65262

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2006-06-29

Regulatory Status

Discontinued

2006

29 Jun

Discontinued Application: 65262

Drug Name

CEFTRIAXONE

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2006-06-29

65262 / 2 View Details

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65262

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2006-06-29

Regulatory Status

Discontinued

2006

01 May

Discontinued Application: 65274

Drug Name

CEFTRIAXONE

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2006-05-01

65274 / 1 View Details

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65274

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2006-05-01

Regulatory Status

Discontinued

1987

24 Apr

Discontinued Application: 62760

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1987-04-24

62760 / 1 View Details

Active Ingredient

CEPHALEXIN

Application Number

62760

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1987-04-24

Regulatory Status

Discontinued

1987

24 Apr

Discontinued Application: 62761

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1987-04-24

62761 / 1 View Details

Active Ingredient

CEPHALEXIN

Application Number

62761

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1987-04-24

Regulatory Status

Discontinued

1987

16 Jun

Discontinued Application: 62767

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1987-06-16

62767 / 1 View Details

Active Ingredient

CEPHALEXIN

Application Number

62767

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1987-06-16

Regulatory Status

Discontinued

1987

16 Jun

Discontinued Application: 62768

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1987-06-16

62768 / 1 View Details

Active Ingredient

CEPHALEXIN

Application Number

62768

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1987-06-16

Regulatory Status

Discontinued

1988

05 Feb

Discontinued Application: 62821

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1988-02-05

62821 / 1 View Details

Active Ingredient

CEPHALEXIN

Application Number

62821

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1988-02-05

Regulatory Status

Discontinued

1988

05 Feb

Discontinued Application: 62823

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1988-02-05

62823 / 1 View Details

Active Ingredient

CEPHALEXIN

Application Number

62823

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1988-02-05

Regulatory Status

Discontinued

1988

15 Apr

Discontinued Application: 62867

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1988-04-15

62867 / 1 View Details

Active Ingredient

CEPHALEXIN

Application Number

62867

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1988-04-15

Regulatory Status

Discontinued

1988

23 May

Discontinued Application: 62873

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1988-05-23

62873 / 1 View Details

Active Ingredient

CEPHALEXIN

Application Number

62873

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1988-05-23

Regulatory Status

Discontinued

1987

09 Jan

Discontinued Application: 62683

Drug Name

CEPHRADINE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1987-01-09

62683 / 1 View Details

Active Ingredient

CEPHRADINE

Application Number

62683

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1987-01-09

Regulatory Status

Discontinued

1987

09 Jan

Discontinued Application: 62683

Drug Name

CEPHRADINE

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1987-01-09

62683 / 2 View Details

Active Ingredient

CEPHRADINE

Application Number

62683

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1987-01-09

Regulatory Status

Discontinued

1987

09 Jan

Discontinued Application: 62693

Drug Name

CEPHRADINE

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1987-01-09

62693 / 1 View Details

Active Ingredient

CEPHRADINE

Application Number

62693

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1987-01-09

Regulatory Status

Discontinued

1987

09 Jan

Discontinued Application: 62693

Drug Name

CEPHRADINE

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1987-01-09

62693 / 2 View Details

Active Ingredient

CEPHRADINE

Application Number

62693

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1987-01-09

Regulatory Status

Discontinued

2011

13 Apr

Discontinued Application: 76447

Drug Name

CHILDRENS FEXOFENADINE HYDROCHLORIDE ALLERGY

Product Number

4

Dosage Form

-

Strength

30MG

Approval Date

2011-04-13

76447 / 4 View Details

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76447

Product Number

4

Dosage Form

-

Strength

30MG

Approval Date

2011-04-13

Regulatory Status

Discontinued

2011

13 Apr

Discontinued Application: 76447

Drug Name

CHILDRENS FEXOFENADINE HYDROCHLORIDE HIVES

Product Number

5

Dosage Form

-

Strength

30MG

Approval Date

2011-04-13

76447 / 5 View Details

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76447

Product Number

5

Dosage Form

-

Strength

30MG

Approval Date

2011-04-13

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86494

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

86494 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

86494

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985

18 Jan

Discontinued Application: 88705

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1985-01-18

88705 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

88705

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1985-01-18

Regulatory Status

Discontinued

1985

18 Jan

Discontinued Application: 88706

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1985-01-18

88706 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

88706

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1985-01-18

Regulatory Status

Discontinued

1985

18 Jan

Discontinued Application: 88707

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-01-18

88707 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

88707

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-01-18

Regulatory Status

Discontinued

1982

13 Jan

Discontinued Application: 87504

Drug Name

CHLOROQUINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-13

87504 / 1 View Details

Active Ingredient

CHLOROQUINE PHOSPHATE

Application Number

87504

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-13

Regulatory Status

Discontinued

1998

28 May

Discontinued Application: 74347

Drug Name

CHOLESTYRAMINE

Product Number

1

Dosage Form

-

Strength

EQ 4GM RESIN/PACKET

Approval Date

1998-05-28

74347 / 1 View Details

Active Ingredient

CHOLESTYRAMINE

Application Number

74347

Product Number

1

Dosage Form

-

Strength

EQ 4GM RESIN/PACKET

Approval Date

1998-05-28

Regulatory Status

Discontinued

1998

28 May

Discontinued Application: 74347

Drug Name

CHOLESTYRAMINE

Product Number

2

Dosage Form

-

Strength

EQ 4GM RESIN/SCOOPFUL

Approval Date

1998-05-28

74347 / 2 View Details

Active Ingredient

CHOLESTYRAMINE

Application Number

74347

Product Number

2

Dosage Form

-

Strength

EQ 4GM RESIN/SCOOPFUL

Approval Date

1998-05-28

Regulatory Status

Discontinued

1998

28 May

Discontinued Application: 74348

Drug Name

CHOLESTYRAMINE LIGHT

Product Number

1

Dosage Form

-

Strength

EQ 4GM RESIN/PACKET

Approval Date

1998-05-28

74348 / 1 View Details

Active Ingredient

CHOLESTYRAMINE

Application Number

74348

Product Number

1

Dosage Form

-

Strength

EQ 4GM RESIN/PACKET

Approval Date

1998-05-28

Regulatory Status

Discontinued

1998

28 May

Discontinued Application: 74348

Drug Name

CHOLESTYRAMINE LIGHT

Product Number

2

Dosage Form

-

Strength

EQ 4GM RESIN/SCOOPFUL

Approval Date

1998-05-28

74348 / 2 View Details

Active Ingredient

CHOLESTYRAMINE

Application Number

74348

Product Number

2

Dosage Form

-

Strength

EQ 4GM RESIN/SCOOPFUL

Approval Date

1998-05-28

Regulatory Status

Discontinued

1995

28 Feb

Discontinued Application: 74365

Drug Name

CIMETIDINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1995-02-28

74365 / 1 View Details

Active Ingredient

CIMETIDINE

Application Number

74365

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1995-02-28

Regulatory Status

Discontinued

1995

28 Feb

Discontinued Application: 74365

Drug Name

CIMETIDINE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

1995-02-28

74365 / 2 View Details

Active Ingredient

CIMETIDINE

Application Number

74365

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

1995-02-28

Regulatory Status

Discontinued

1995

28 Feb

Discontinued Application: 74365

Drug Name

CIMETIDINE

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

1995-02-28

74365 / 3 View Details

Active Ingredient

CIMETIDINE

Application Number

74365

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

1995-02-28

Regulatory Status

Discontinued

1995

28 Feb

Discontinued Application: 74365

Drug Name

CIMETIDINE

Product Number

4

Dosage Form

-

Strength

800MG

Approval Date

1995-02-28

74365 / 4 View Details

Active Ingredient

CIMETIDINE

Application Number

74365

Product Number

4

Dosage Form

-

Strength

800MG

Approval Date

1995-02-28

Regulatory Status

Discontinued

1992

28 Feb

Discontinued Application: 73005

Drug Name

CINOXACIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1992-02-28

73005 / 1 View Details

Active Ingredient

CINOXACIN

Application Number

73005

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1992-02-28

Regulatory Status

Discontinued

1992

28 Feb

Discontinued Application: 73006

Drug Name

CINOXACIN

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1992-02-28

73006 / 1 View Details

Active Ingredient

CINOXACIN

Application Number

73006

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1992-02-28

Regulatory Status

Discontinued

2004

09 Jun

Discontinued Application: 76136

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-06-09

76136 / 1 View Details

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76136

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-06-09

Regulatory Status

Discontinued

2004

09 Jun

Discontinued Application: 76136

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-06-09

76136 / 2 View Details

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76136

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-06-09

Regulatory Status

Discontinued

2004

09 Jun

Discontinued Application: 76136

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

76136 / 3 View Details

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76136

Product Number

3

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

Regulatory Status

Discontinued

2005

31 May

Discontinued Application: 65155

Drug Name

CLARITHROMYCIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2005-05-31

65155 / 1 View Details

Active Ingredient

CLARITHROMYCIN

Application Number

65155

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2005-05-31

Regulatory Status

Discontinued

2005

31 May

Discontinued Application: 65155

Drug Name

CLARITHROMYCIN

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2005-05-31

65155 / 2 View Details

Active Ingredient

CLARITHROMYCIN

Application Number

65155

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2005-05-31

Regulatory Status

Discontinued

1989

20 Sep

Discontinued Application: 63027

Drug Name

CLINDAMYCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1989-09-20

63027 / 1 View Details

Active Ingredient

CLINDAMYCIN HYDROCHLORIDE

Application Number

63027

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1989-09-20

Regulatory Status

Discontinued

1991

25 Jul

Discontinued Application: 72600

Drug Name

CLOFIBRATE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1991-07-25

72600 / 1 View Details

Active Ingredient

CLOFIBRATE

Application Number

72600

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1991-07-25

Regulatory Status

Discontinued

1997

04 Apr

Discontinued Application: 74849

Drug Name

CLOMIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1997-04-04

74849 / 1 View Details

Active Ingredient

CLOMIPRAMINE HYDROCHLORIDE

Application Number

74849

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1997-04-04

Regulatory Status

Discontinued

1997

04 Apr

Discontinued Application: 74849

Drug Name

CLOMIPRAMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1997-04-04

74849 / 2 View Details

Active Ingredient

CLOMIPRAMINE HYDROCHLORIDE

Application Number

74849

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1997-04-04

Regulatory Status

Discontinued

1997

04 Apr

Discontinued Application: 74849

Drug Name

CLOMIPRAMINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

1997-04-04

74849 / 3 View Details

Active Ingredient

CLOMIPRAMINE HYDROCHLORIDE

Application Number

74849

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

1997-04-04

Regulatory Status

Discontinued

1997

26 Aug

Discontinued Application: 74958

Drug Name

CLOMIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1997-08-26

74958 / 1 View Details

Active Ingredient

CLOMIPRAMINE HYDROCHLORIDE

Application Number

74958

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1997-08-26

Regulatory Status

Discontinued

1997

26 Aug

Discontinued Application: 74958

Drug Name

CLOMIPRAMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1997-08-26

74958 / 2 View Details

Active Ingredient

CLOMIPRAMINE HYDROCHLORIDE

Application Number

74958

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1997-08-26

Regulatory Status

Discontinued

1997

26 Aug

Discontinued Application: 74958

Drug Name

CLOMIPRAMINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

1997-08-26

74958 / 3 View Details

Active Ingredient

CLOMIPRAMINE HYDROCHLORIDE

Application Number

74958

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

1997-08-26

Regulatory Status

Discontinued

1998

04 Aug

Discontinued Application: 74920

Drug Name

CLONAZEPAM

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1998-08-04

74920 / 1 View Details

Active Ingredient

CLONAZEPAM

Application Number

74920

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1998-08-04

Regulatory Status

Discontinued

1998

04 Aug

Discontinued Application: 74920

Drug Name

CLONAZEPAM

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

1998-08-04

74920 / 2 View Details

Active Ingredient

CLONAZEPAM

Application Number

74920

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

1998-08-04

Regulatory Status

Discontinued

1998

04 Aug

Discontinued Application: 74920

Drug Name

CLONAZEPAM

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

1998-08-04

74920 / 3 View Details

Active Ingredient

CLONAZEPAM

Application Number

74920

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

1998-08-04

Regulatory Status

Discontinued

1986

08 Jul

Discontinued Application: 70659

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

1986-07-08

70659 / 1 View Details

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

70659

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

1986-07-08

Regulatory Status

Discontinued

1986

08 Jul

Discontinued Application: 70702

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.2MG

Approval Date

1986-07-08

70702 / 1 View Details

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

70702

Product Number

1

Dosage Form

-

Strength

0.2MG

Approval Date

1986-07-08

Regulatory Status

Discontinued

1986

08 Jul

Discontinued Application: 70747

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1986-07-08

70747 / 1 View Details

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

70747

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1986-07-08

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62240

Drug Name

CLOXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

62240 / 1 View Details

Active Ingredient

CLOXACILLIN SODIUM

Application Number

62240

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62240

Drug Name

CLOXACILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

62240 / 2 View Details

Active Ingredient

CLOXACILLIN SODIUM

Application Number

62240

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62268

Drug Name

CLOXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

62268 / 1 View Details

Active Ingredient

CLOXACILLIN SODIUM

Application Number

62268

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989

06 Apr

Discontinued Application: 62978

Drug Name

CLOXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1989-04-06

62978 / 1 View Details

Active Ingredient

CLOXACILLIN SODIUM

Application Number

62978

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1989-04-06

Regulatory Status

Discontinued

1985

16 May

Discontinued Application: 70034

Drug Name

COTRIM

Product Number

1

Dosage Form

-

Strength

400MG;80MG

Approval Date

1985-05-16

70034 / 1 View Details

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70034

Product Number

1

Dosage Form

-

Strength

400MG;80MG

Approval Date

1985-05-16

Regulatory Status

Discontinued

1985

18 Mar

Discontinued Application: 70048

Drug Name

COTRIM D.S.

Product Number

1

Dosage Form

-

Strength

800MG;160MG

Approval Date

1985-03-18

70048 / 1 View Details

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70048

Product Number

1

Dosage Form

-

Strength

800MG;160MG

Approval Date

1985-03-18

Regulatory Status

Discontinued

1988

04 Aug

Discontinued Application: 62895

Drug Name

CYCLACILLIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1988-08-04

62895 / 1 View Details

Active Ingredient

CYCLACILLIN

Application Number

62895

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1988-08-04

Regulatory Status

Discontinued

1988

04 Aug

Discontinued Application: 62895

Drug Name

CYCLACILLIN

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1988-08-04

62895 / 2 View Details

Active Ingredient

CYCLACILLIN

Application Number

62895

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1988-08-04

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83563

Drug Name

DELCOBESE

Product Number

1

Dosage Form

-

Strength

5MG;5MG;5MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

83563 / 1 View Details

Active Ingredient

AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE

Application Number

83563

Product Number

1

Dosage Form

-

Strength

5MG;5MG;5MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83563

Drug Name

DELCOBESE

Product Number

2

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

83563 / 2 View Details

Active Ingredient

AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE

Application Number

83563

Product Number

2

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83563

Drug Name

DELCOBESE

Product Number

3

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

83563 / 3 View Details

Active Ingredient

AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE

Application Number

83563

Product Number

3

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83563

Drug Name

DELCOBESE

Product Number

4

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

83563 / 4 View Details

Active Ingredient

AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE

Application Number

83563

Product Number

4

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83564

Drug Name

DELCOBESE

Product Number

1

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

83564 / 1 View Details

Active Ingredient

AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE

Application Number

83564

Product Number

1

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83564

Drug Name

DELCOBESE

Product Number

2

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

83564 / 2 View Details

Active Ingredient

AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE

Application Number

83564

Product Number

2

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83564

Drug Name

DELCOBESE

Product Number

3

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

83564 / 3 View Details

Active Ingredient

AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE

Application Number

83564

Product Number

3

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83564

Drug Name

DELCOBESE

Product Number

4

Dosage Form

-

Strength

5MG;5MG;5MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

83564 / 4 View Details

Active Ingredient

AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE

Application Number

83564

Product Number

4

Dosage Form

-

Strength

5MG;5MG;5MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83735

Drug Name

DEXAMPEX

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

83735 / 1 View Details

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

83735

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83735

Drug Name

DEXAMPEX

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

83735 / 2 View Details

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

83735

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85355

Drug Name

DEXAMPEX

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1982-01-01

85355 / 1 View Details

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

85355

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2013

29 Apr

Discontinued Application: 77488

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

2013-04-29

77488 / 1 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

77488

Product Number

1

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG

Approval Date

2013-04-29

Regulatory Status

Discontinued

2013

29 Apr

Discontinued Application: 77488

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

2013-04-29

77488 / 2 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

77488

Product Number

2

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG

Approval Date

2013-04-29

Regulatory Status

Discontinued

2013

29 Apr

Discontinued Application: 77488

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

2013-04-29

77488 / 3 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

77488

Product Number

3

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG

Approval Date

2013-04-29

Regulatory Status

Discontinued

2013

29 Apr

Discontinued Application: 77488

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

4

Dosage Form

-

Strength

5MG;5MG;5MG;5MG

Approval Date

2013-04-29

77488 / 4 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

77488

Product Number

4

Dosage Form

-

Strength

5MG;5MG;5MG;5MG

Approval Date

2013-04-29

Regulatory Status

Discontinued

2013

29 Apr

Discontinued Application: 77488

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

2013-04-29

77488 / 5 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

77488

Product Number

5

Dosage Form

-

Strength

6.25MG;6.25MG;6.25MG;6.25MG

Approval Date

2013-04-29

Regulatory Status

Discontinued

2013

29 Apr

Discontinued Application: 77488

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

2013-04-29

77488 / 6 View Details

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

77488

Product Number

6

Dosage Form

-

Strength

7.5MG;7.5MG;7.5MG;7.5MG

Approval Date

2013-04-29

Regulatory Status

Discontinued

1996

15 Aug

Discontinued Application: 74390

Drug Name

DICLOFENAC SODIUM

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1996-08-15

74390 / 1 View Details

Active Ingredient

DICLOFENAC SODIUM

Application Number

74390

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1996-08-15

Regulatory Status

Discontinued

1999

30 Mar

Discontinued Application: 74723

Drug Name

DICLOFENAC SODIUM

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1999-03-30

74723 / 1 View Details

Active Ingredient

DICLOFENAC SODIUM

Application Number

74723

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1999-03-30

Regulatory Status

Discontinued

1984

20 Sep

Discontinued Application: 88642

Drug Name

DIETHYLPROPION HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1984-09-20

88642 / 1 View Details

Active Ingredient

DIETHYLPROPION HYDROCHLORIDE

Application Number

88642

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1984-09-20

Regulatory Status

Discontinued

1992

31 Jul

Discontinued Application: 73679

Drug Name

DIFLUNISAL

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1992-07-31

73679 / 1 View Details

Active Ingredient

DIFLUNISAL

Application Number

73679

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1992-07-31

Regulatory Status

Discontinued

1993

30 Nov

Discontinued Application: 74079

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

1993-11-30

74079 / 1 View Details

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

74079

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

1993-11-30

Regulatory Status

Discontinued

1993

30 Nov

Discontinued Application: 74079

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

90MG

Approval Date

1993-11-30

74079 / 2 View Details

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

74079

Product Number

2

Dosage Form

-

Strength

90MG

Approval Date

1993-11-30

Regulatory Status

Discontinued

1993

30 Nov

Discontinued Application: 74079

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

120MG

Approval Date

1993-11-30

74079 / 3 View Details

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

74079

Product Number

3

Dosage Form

-

Strength

120MG

Approval Date

1993-11-30

Regulatory Status

Discontinued

1994

25 Feb

Discontinued Application: 74084

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1994-02-25

74084 / 1 View Details

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

74084

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1994-02-25

Regulatory Status

Discontinued

1994

25 Feb

Discontinued Application: 74084

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

1994-02-25

74084 / 2 View Details

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

74084

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

1994-02-25

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85874

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

85874 / 1 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

85874

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85874

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

85874 / 2 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

85874

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2008

29 Jul

Discontinued Application: 76941

Drug Name

DIVALPROEX SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 125MG VALPROIC ACID

Approval Date

2008-07-29

76941 / 1 View Details

Active Ingredient

DIVALPROEX SODIUM

Application Number

76941

Product Number

1

Dosage Form

-

Strength

EQ 125MG VALPROIC ACID

Approval Date

2008-07-29

Regulatory Status

Discontinued

2008

29 Jul

Discontinued Application: 76941

Drug Name

DIVALPROEX SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 250MG VALPROIC ACID

Approval Date

2008-07-29

76941 / 2 View Details

Active Ingredient

DIVALPROEX SODIUM

Application Number

76941

Product Number

2

Dosage Form

-

Strength

EQ 250MG VALPROIC ACID

Approval Date

2008-07-29

Regulatory Status

Discontinued

2008

29 Jul

Discontinued Application: 76941

Drug Name

DIVALPROEX SODIUM

Product Number

3

Dosage Form

-

Strength

EQ 500MG VALPROIC ACID

Approval Date

2008-07-29

76941 / 3 View Details

Active Ingredient

DIVALPROEX SODIUM

Application Number

76941

Product Number

3

Dosage Form

-

Strength

EQ 500MG VALPROIC ACID

Approval Date

2008-07-29

Regulatory Status

Discontinued

2001

12 Jan

Discontinued Application: 75353

Drug Name

DOXAZOSIN MESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2001-01-12

75353 / 1 View Details

Active Ingredient

DOXAZOSIN MESYLATE

Application Number

75353

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2001-01-12

Regulatory Status

Discontinued

2001

12 Jan

Discontinued Application: 75353

Drug Name

DOXAZOSIN MESYLATE

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2001-01-12

75353 / 2 View Details

Active Ingredient

DOXAZOSIN MESYLATE

Application Number

75353

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2001-01-12

Regulatory Status

Discontinued

2001

12 Jan

Discontinued Application: 75353

Drug Name

DOXAZOSIN MESYLATE

Product Number

3

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2001-01-12

75353 / 3 View Details

Active Ingredient

DOXAZOSIN MESYLATE

Application Number

75353

Product Number

3

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2001-01-12

Regulatory Status

Discontinued

2001

12 Jan

Discontinued Application: 75353

Drug Name

DOXAZOSIN MESYLATE

Product Number

4

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2001-01-12

75353 / 4 View Details

Active Ingredient

DOXAZOSIN MESYLATE

Application Number

75353

Product Number

4

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2001-01-12

Regulatory Status

Discontinued

1984

23 Aug

Discontinued Application: 62497

Drug Name

DOXY-LEMMON

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1984-08-23

62497 / 1 View Details

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62497

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1984-08-23

Regulatory Status

Discontinued

1984

15 Jun

Discontinued Application: 62497

Drug Name

DOXY-LEMMON

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1984-06-15

62497 / 2 View Details

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62497

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1984-06-15

Regulatory Status

Discontinued

1985

15 Mar

Discontinued Application: 62581

Drug Name

DOXY-LEMMON

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1985-03-15

62581 / 1 View Details

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62581

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1985-03-15

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84301

Drug Name

DRALZINE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

84301 / 1 View Details

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

84301

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1999

23 Apr

Discontinued Application: 74847

Drug Name

ETODOLAC

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1999-04-23

74847 / 1 View Details

Active Ingredient

ETODOLAC

Application Number

74847

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1999-04-23

Regulatory Status

Discontinued

1999

23 Apr

Discontinued Application: 74847

Drug Name

ETODOLAC

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1999-04-23

74847 / 2 View Details

Active Ingredient

ETODOLAC

Application Number

74847

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1999-04-23

Regulatory Status

Discontinued

1997

26 Nov

Discontinued Application: 75009

Drug Name

ETODOLAC

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1997-11-26

75009 / 1 View Details

Active Ingredient

ETODOLAC

Application Number

75009

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1997-11-26

Regulatory Status

Discontinued

1999

28 Dec

Discontinued Application: 75009

Drug Name

ETODOLAC

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1999-12-28

75009 / 2 View Details

Active Ingredient

ETODOLAC

Application Number

75009

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1999-12-28

Regulatory Status

Discontinued

2001

16 Apr

Discontinued Application: 75311

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2001-04-16

75311 / 1 View Details

Active Ingredient

FAMOTIDINE

Application Number

75311

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2001-04-16

Regulatory Status

Discontinued

2001

16 Apr

Discontinued Application: 75311

Drug Name

FAMOTIDINE

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2001-04-16

75311 / 2 View Details

Active Ingredient

FAMOTIDINE

Application Number

75311

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2001-04-16

Regulatory Status

Discontinued

2001

31 May

Discontinued Application: 75312

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2001-05-31

75312 / 1 View Details

Active Ingredient

FAMOTIDINE

Application Number

75312

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2001-05-31

Regulatory Status

Discontinued

2005

01 Sep

Discontinued Application: 76447

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2005-09-01

76447 / 1 View Details

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76447

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2005-09-01

Regulatory Status

Discontinued

2005

01 Sep

Discontinued Application: 76447

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

2005-09-01

76447 / 2 View Details

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76447

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

2005-09-01

Regulatory Status

Discontinued

2005

01 Sep

Discontinued Application: 76447

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

180MG

Approval Date

2005-09-01

76447 / 3 View Details

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76447

Product Number

3

Dosage Form

-

Strength

180MG

Approval Date

2005-09-01

Regulatory Status

Discontinued

2011

13 Apr

Discontinued Application: 76447

Drug Name

FEXOFENADINE HYDROCHLORIDE ALLERGY

Product Number

6

Dosage Form

-

Strength

60MG

Approval Date

2011-04-13

76447 / 6 View Details

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76447

Product Number

6

Dosage Form

-

Strength

60MG

Approval Date

2011-04-13

Regulatory Status

Discontinued

2011

13 Apr

Discontinued Application: 76447

Drug Name

FEXOFENADINE HYDROCHLORIDE ALLERGY

Product Number

8

Dosage Form

-

Strength

180MG

Approval Date

2011-04-13

76447 / 8 View Details

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76447

Product Number

8

Dosage Form

-

Strength

180MG

Approval Date

2011-04-13

Regulatory Status

Discontinued

2011

13 Apr

Discontinued Application: 76447

Drug Name

FEXOFENADINE HYDROCHLORIDE HIVES

Product Number

7

Dosage Form

-

Strength

60MG

Approval Date

2011-04-13

76447 / 7 View Details

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76447

Product Number

7

Dosage Form

-

Strength

60MG

Approval Date

2011-04-13

Regulatory Status

Discontinued

2013

05 Nov

Discontinued Application: 76905

Drug Name

FINASTERIDE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2013-11-05

76905 / 1 View Details

Active Ingredient

FINASTERIDE

Application Number

76905

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2013-11-05

Regulatory Status

Discontinued

2004

29 Jul

Discontinued Application: 74681

Drug Name

FLUCONAZOLE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2004-07-29

74681 / 1 View Details

Active Ingredient

FLUCONAZOLE

Application Number

74681

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2004

29 Jul

Discontinued Application: 74681

Drug Name

FLUCONAZOLE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2004-07-29

74681 / 2 View Details

Active Ingredient

FLUCONAZOLE

Application Number

74681

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2004

29 Jul

Discontinued Application: 74681

Drug Name

FLUCONAZOLE

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2004-07-29

74681 / 3 View Details

Active Ingredient

FLUCONAZOLE

Application Number

74681

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2004

29 Jul

Discontinued Application: 74681

Drug Name

FLUCONAZOLE

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2004-07-29

74681 / 4 View Details

Active Ingredient

FLUCONAZOLE

Application Number

74681

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

1989

07 Feb

Discontinued Application: 72511

Drug Name

FLUOCINONIDE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

1989-02-07

72511 / 1 View Details

Active Ingredient

FLUOCINONIDE

Application Number

72511

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

1989-02-07

Regulatory Status

Discontinued

2002

29 Jan

Discontinued Application: 75872

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-29

75872 / 1 View Details

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75872

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-29

Regulatory Status

Discontinued

2019

04 Jan

Discontinued Application: 75872

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2019-01-04

75872 / 2 View Details

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75872

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2019-01-04

Regulatory Status

Discontinued

1995

24 May

Discontinued Application: 74405

Drug Name

FLURBIPROFEN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1995-05-24

74405 / 1 View Details

Active Ingredient

FLURBIPROFEN

Application Number

74405

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1995-05-24

Regulatory Status

Discontinued

1995

24 May

Discontinued Application: 74405

Drug Name

FLURBIPROFEN

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1995-05-24

74405 / 2 View Details

Active Ingredient

FLURBIPROFEN

Application Number

74405

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1995-05-24

Regulatory Status

Discontinued

2002

10 Sep

Discontinued Application: 75893

Drug Name

FLUVOXAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2002-09-10

75893 / 1 View Details

Active Ingredient

FLUVOXAMINE MALEATE

Application Number

75893

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2002-09-10

Regulatory Status

Discontinued

2002

10 Sep

Discontinued Application: 75893

Drug Name

FLUVOXAMINE MALEATE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2002-09-10

75893 / 2 View Details

Active Ingredient

FLUVOXAMINE MALEATE

Application Number

75893

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2002-09-10

Regulatory Status

Discontinued

2002

10 Sep

Discontinued Application: 75893

Drug Name

FLUVOXAMINE MALEATE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2002-09-10

75893 / 3 View Details

Active Ingredient

FLUVOXAMINE MALEATE

Application Number

75893

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2002-09-10

Regulatory Status

Discontinued

2006

05 Jul

Discontinued Application: 76945

Drug Name

FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

10MG;12.5MG

Approval Date

2006-07-05

76945 / 1 View Details

Active Ingredient

FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

Application Number

76945

Product Number

1

Dosage Form

-

Strength

10MG;12.5MG

Approval Date

2006-07-05

Regulatory Status

Discontinued

2006

05 Jul

Discontinued Application: 76945

Drug Name

FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

20MG;12.5MG

Approval Date

2006-07-05

76945 / 2 View Details

Active Ingredient

FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

Application Number

76945

Product Number

2

Dosage Form

-

Strength

20MG;12.5MG

Approval Date

2006-07-05

Regulatory Status

Discontinued

2004

15 Dec

Discontinued Application: 75827

Drug Name

GABAPENTIN

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2004-12-15

75827 / 1 View Details

Active Ingredient

GABAPENTIN

Application Number

75827

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2004-12-15

Regulatory Status

Discontinued

2004

15 Dec

Discontinued Application: 75827

Drug Name

GABAPENTIN

Product Number

2

Dosage Form

-

Strength

800MG

Approval Date

2004-12-15

75827 / 2 View Details

Active Ingredient

GABAPENTIN

Application Number

75827

Product Number

2

Dosage Form

-

Strength

800MG

Approval Date

2004-12-15

Regulatory Status

Discontinued

1993

31 Oct

Discontinued Application: 74256

Drug Name

GEMFIBROZIL

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1993-10-31

74256 / 1 View Details

Active Ingredient

GEMFIBROZIL

Application Number

74256

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1993-10-31

Regulatory Status

Discontinued

2005

27 Jan

Discontinued Application: 76821

Drug Name

GLYBURIDE AND METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1.25MG;250MG

Approval Date

2005-01-27

76821 / 1 View Details

Active Ingredient

GLYBURIDE; METFORMIN HYDROCHLORIDE

Application Number

76821

Product Number

1

Dosage Form

-

Strength

1.25MG;250MG

Approval Date

2005-01-27

Regulatory Status

Discontinued

2005

27 Jan

Discontinued Application: 76821

Drug Name

GLYBURIDE AND METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

2.5MG;500MG

Approval Date

2005-01-27

76821 / 2 View Details

Active Ingredient

GLYBURIDE; METFORMIN HYDROCHLORIDE

Application Number

76821

Product Number

2

Dosage Form

-

Strength

2.5MG;500MG

Approval Date

2005-01-27

Regulatory Status

Discontinued

2005

27 Jan

Discontinued Application: 76821

Drug Name

GLYBURIDE AND METFORMIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

5MG;500MG

Approval Date

2005-01-27

76821 / 3 View Details

Active Ingredient

GLYBURIDE; METFORMIN HYDROCHLORIDE

Application Number

76821

Product Number

3

Dosage Form

-

Strength

5MG;500MG

Approval Date

2005-01-27

Regulatory Status

Discontinued

1987

25 Aug

Discontinued Application: 71015

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

1987-08-25

71015 / 1 View Details

Active Ingredient

HALOPERIDOL LACTATE

Application Number

71015

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

1987-08-25

Regulatory Status

Discontinued

1985

04 Mar

Discontinued Application: 88713

Drug Name

HY-PAM "25"

Product Number

1

Dosage Form

-

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1985-03-04

88713 / 1 View Details

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

88713

Product Number

1

Dosage Form

-

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1985-03-04

Regulatory Status

Discontinued

1985

07 Feb

Discontinued Application: 88923

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1985-02-07

88923 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

88923

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1985-02-07

Regulatory Status

Discontinued

1985

07 Feb

Discontinued Application: 88924

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-02-07

88924 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

88924

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-02-07

Regulatory Status

Discontinued

2003

11 Apr

Discontinued Application: 76023

Drug Name

HYDROCODONE BITARTRATE AND IBUPROFEN

Product Number

1

Dosage Form

-

Strength

7.5MG;200MG

Approval Date

2003-04-11

76023 / 1 View Details

Active Ingredient

HYDROCODONE BITARTRATE; IBUPROFEN

Application Number

76023

Product Number

1

Dosage Form

-

Strength

7.5MG;200MG

Approval Date

2003-04-11

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80400

Drug Name

HYDROCORTISONE

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

80400 / 2 View Details

Active Ingredient

HYDROCORTISONE

Application Number

80400

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80400

Drug Name

HYDROCORTISONE

Product Number

3

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

80400 / 3 View Details

Active Ingredient

HYDROCORTISONE

Application Number

80400

Product Number

3

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80400

Drug Name

HYDROCORTISONE

Product Number

4

Dosage Form

-

Strength

2.5%

Approval Date

1982-01-01

80400 / 4 View Details

Active Ingredient

HYDROCORTISONE

Application Number

80400

Product Number

4

Dosage Form

-

Strength

2.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85191

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

85191 / 1 View Details

Active Ingredient

HYDROCORTISONE

Application Number

85191

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1992

29 May

Discontinued Application: 73141

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1992-05-29

73141 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

73141

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1992-05-29

Regulatory Status

Discontinued

1992

30 Jun

Discontinued Application: 73343

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1992-06-30

73343 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

73343

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1992-06-30

Regulatory Status

Discontinued

1992

30 Jun

Discontinued Application: 73344

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1992-06-30

73344 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

73344

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1992-06-30

Regulatory Status

Discontinued

1992

30 Jun

Discontinued Application: 73345

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

1992-06-30

73345 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

73345

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

1992-06-30

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83729

Drug Name

IMIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

83729 / 1 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

83729

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83729

Drug Name

IMIPRAMINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

83729 / 3 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

83729

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83729

Drug Name

IMIPRAMINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

83729 / 4 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

83729

Product Number

4

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1997

04 Apr

Discontinued Application: 74665

Drug Name

INDAPAMIDE

Product Number

1

Dosage Form

-

Strength

1.25MG

Approval Date

1997-04-04

74665 / 1 View Details

Active Ingredient

INDAPAMIDE

Application Number

74665

Product Number

1

Dosage Form

-

Strength

1.25MG

Approval Date

1997-04-04

Regulatory Status

Discontinued

1997

04 Apr

Discontinued Application: 74665

Drug Name

INDAPAMIDE

Product Number

2

Dosage Form

-

Strength

2.5MG

Approval Date

1997-04-04

74665 / 2 View Details

Active Ingredient

INDAPAMIDE

Application Number

74665

Product Number

2

Dosage Form

-

Strength

2.5MG

Approval Date

1997-04-04

Regulatory Status

Discontinued

1985

07 Nov

Discontinued Application: 70266

Drug Name

INDO-LEMMON

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-11-07

70266 / 1 View Details

Active Ingredient

INDOMETHACIN

Application Number

70266

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-11-07

Regulatory Status

Discontinued

1985

07 Nov

Discontinued Application: 70267

Drug Name

INDO-LEMMON

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1985-11-07

70267 / 1 View Details

Active Ingredient

INDOMETHACIN

Application Number

70267

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1985-11-07

Regulatory Status

Discontinued

1988

18 Apr

Discontinued Application: 71342

Drug Name

INDOMETHACIN

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1988-04-18

71342 / 1 View Details

Active Ingredient

INDOMETHACIN

Application Number

71342

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1988-04-18

Regulatory Status

Discontinued

1988

18 Apr

Discontinued Application: 71343

Drug Name

INDOMETHACIN

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1988-04-18

71343 / 1 View Details

Active Ingredient

INDOMETHACIN

Application Number

71343

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1988-04-18

Regulatory Status

Discontinued

2012

30 Mar

Discontinued Application: 77369

Drug Name

IRBESARTAN AND HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

25MG;300MG

Approval Date

2012-03-30

77369 / 3 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE; IRBESARTAN

Application Number

77369

Product Number

3

Dosage Form

-

Strength

25MG;300MG

Approval Date

2012-03-30

Regulatory Status

Discontinued

1999

15 Jun

Discontinued Application: 75273

Drug Name

KETOCONAZOLE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1999-06-15

75273 / 1 View Details

Active Ingredient

KETOCONAZOLE

Application Number

75273

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1999-06-15

Regulatory Status

Discontinued

1992

22 Dec

Discontinued Application: 73515

Drug Name

KETOPROFEN

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1992-12-22

73515 / 1 View Details

Active Ingredient

KETOPROFEN

Application Number

73515

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1992-12-22

Regulatory Status

Discontinued

1992

22 Dec

Discontinued Application: 73517

Drug Name

KETOPROFEN

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1992-12-22

73517 / 1 View Details

Active Ingredient

KETOPROFEN

Application Number

73517

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1992-12-22

Regulatory Status

Discontinued

1998

30 Sep

Discontinued Application: 74989

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1998-09-30

74989 / 1 View Details

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

74989

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1998-09-30

Regulatory Status

Discontinued

1998

30 Sep

Discontinued Application: 74989

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

1998-09-30

74989 / 2 View Details

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

74989

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

1998-09-30

Regulatory Status

Discontinued

1998

30 Sep

Discontinued Application: 74989

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

1998-09-30

74989 / 3 View Details

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

74989

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

1998-09-30

Regulatory Status

Discontinued

2006

30 Aug

Discontinued Application: 76388

Drug Name

LAMOTRIGINE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2006-08-30

76388 / 1 View Details

Active Ingredient

LAMOTRIGINE

Application Number

76388

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2006-08-30

Regulatory Status

Discontinued

2006

30 Aug

Discontinued Application: 76388

Drug Name

LAMOTRIGINE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2006-08-30

76388 / 2 View Details

Active Ingredient

LAMOTRIGINE

Application Number

76388

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2006-08-30

Regulatory Status

Discontinued

2006

30 Aug

Discontinued Application: 76388

Drug Name

LAMOTRIGINE

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2006-08-30

76388 / 3 View Details

Active Ingredient

LAMOTRIGINE

Application Number

76388

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2006-08-30

Regulatory Status

Discontinued

2006

30 Aug

Discontinued Application: 76388

Drug Name

LAMOTRIGINE

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2006-08-30

76388 / 4 View Details

Active Ingredient

LAMOTRIGINE

Application Number

76388

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2006-08-30

Regulatory Status

Discontinued

2006

21 Jun

Discontinued Application: 76420

Drug Name

LAMOTRIGINE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2006-06-21

76420 / 1 View Details

Active Ingredient

LAMOTRIGINE

Application Number

76420

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2006-06-21

Regulatory Status

Discontinued

2006

21 Jun

Discontinued Application: 76420

Drug Name

LAMOTRIGINE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2006-06-21

76420 / 2 View Details

Active Ingredient

LAMOTRIGINE

Application Number

76420

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2006-06-21

Regulatory Status

Discontinued

2002

01 Jul

Discontinued Application: 75783

Drug Name

LISINOPRIL

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2002-07-01

75783 / 1 View Details

Active Ingredient

LISINOPRIL

Application Number

75783

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2002-07-01

Regulatory Status

Discontinued

2002

01 Jul

Discontinued Application: 75783

Drug Name

LISINOPRIL

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2002-07-01

75783 / 2 View Details

Active Ingredient

LISINOPRIL

Application Number

75783

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2002-07-01

Regulatory Status

Discontinued

2002

01 Jul

Discontinued Application: 75783

Drug Name

LISINOPRIL

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2002-07-01

75783 / 3 View Details

Active Ingredient

LISINOPRIL

Application Number

75783

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2002-07-01

Regulatory Status

Discontinued

2002

01 Jul

Discontinued Application: 75783

Drug Name

LISINOPRIL

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2002-07-01

75783 / 4 View Details

Active Ingredient

LISINOPRIL

Application Number

75783

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2002-07-01

Regulatory Status

Discontinued

2002

01 Jul

Discontinued Application: 75783

Drug Name

LISINOPRIL

Product Number

5

Dosage Form

-

Strength

30MG

Approval Date

2002-07-01

75783 / 5 View Details

Active Ingredient

LISINOPRIL

Application Number

75783

Product Number

5

Dosage Form

-

Strength

30MG

Approval Date

2002-07-01

Regulatory Status

Discontinued

2002

01 Jul

Discontinued Application: 75783

Drug Name

LISINOPRIL

Product Number

6

Dosage Form

-

Strength

40MG

Approval Date

2002-07-01

75783 / 6 View Details

Active Ingredient

LISINOPRIL

Application Number

75783

Product Number

6

Dosage Form

-

Strength

40MG

Approval Date

2002-07-01

Regulatory Status

Discontinued

2002

01 Jul

Discontinued Application: 75869

Drug Name

LISINOPRIL AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

12.5MG;10MG

Approval Date

2002-07-01

75869 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE; LISINOPRIL

Application Number

75869

Product Number

1

Dosage Form

-

Strength

12.5MG;10MG

Approval Date

2002-07-01

Regulatory Status

Discontinued

2002

01 Jul

Discontinued Application: 75869

Drug Name

LISINOPRIL AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

12.5MG;20MG

Approval Date

2002-07-01

75869 / 2 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE; LISINOPRIL

Application Number

75869

Product Number

2

Dosage Form

-

Strength

12.5MG;20MG

Approval Date

2002-07-01

Regulatory Status

Discontinued

2002

01 Jul

Discontinued Application: 75869

Drug Name

LISINOPRIL AND HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

25MG;20MG

Approval Date

2002-07-01

75869 / 3 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE; LISINOPRIL

Application Number

75869

Product Number

3

Dosage Form

-

Strength

25MG;20MG

Approval Date

2002-07-01

Regulatory Status

Discontinued

1991

30 Aug

Discontinued Application: 73122

Drug Name

LOPERAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1991-08-30

73122 / 1 View Details

Active Ingredient

LOPERAMIDE HYDROCHLORIDE

Application Number

73122

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1991-08-30

Regulatory Status

Discontinued

1995

23 Jun

Discontinued Application: 73478

Drug Name

LOPERAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1MG/5ML

Approval Date

1995-06-23

73478 / 1 View Details

Active Ingredient

LOPERAMIDE HYDROCHLORIDE

Application Number

73478

Product Number

1

Dosage Form

-

Strength

1MG/5ML

Approval Date

1995-06-23

Regulatory Status

Discontinued

2003

07 Nov

Discontinued Application: 75505

Drug Name

LORATADINE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2003-11-07

75505 / 1 View Details

Active Ingredient

LORATADINE

Application Number

75505

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2003-11-07

Regulatory Status

Discontinued

2010

06 Apr

Discontinued Application: 76958

Drug Name

LOSARTAN POTASSIUM

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2010-04-06

76958 / 1 View Details

Active Ingredient

LOSARTAN POTASSIUM

Application Number

76958

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2010-04-06

Regulatory Status

Discontinued

2010

06 Apr

Discontinued Application: 76958

Drug Name

LOSARTAN POTASSIUM

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2010-04-06

76958 / 2 View Details

Active Ingredient

LOSARTAN POTASSIUM

Application Number

76958

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2010-04-06

Regulatory Status

Discontinued

2010

06 Apr

Discontinued Application: 76958

Drug Name

LOSARTAN POTASSIUM

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2010-04-06

76958 / 3 View Details

Active Ingredient

LOSARTAN POTASSIUM

Application Number

76958

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2010-04-06

Regulatory Status

Discontinued

1998

27 Feb

Discontinued Application: 74745

Drug Name

MEGESTROL ACETATE

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1998-02-27

74745 / 1 View Details

Active Ingredient

MEGESTROL ACETATE

Application Number

74745

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1998-02-27

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16069

Drug Name

MEPRIAM

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

16069 / 1 View Details

Active Ingredient

MEPROBAMATE

Application Number

16069

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2002

16 Dec

Discontinued Application: 76328

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2002-12-16

76328 / 1 View Details

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

76328

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2002-12-16

Regulatory Status

Discontinued

2002

16 Dec

Discontinued Application: 76328

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2002-12-16

76328 / 2 View Details

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

76328

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2002-12-16

Regulatory Status

Discontinued

2002

16 Dec

Discontinued Application: 76328

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2002-12-16

76328 / 3 View Details

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

76328

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2002-12-16

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83889

Drug Name

METHAMPEX

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

83889 / 1 View Details

Active Ingredient

METHAMPHETAMINE HYDROCHLORIDE

Application Number

83889

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86359

Drug Name

METHAMPHETAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

86359 / 1 View Details

Active Ingredient

METHAMPHETAMINE HYDROCHLORIDE

Application Number

86359

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

05 Dec

Discontinued Application: 71067

Drug Name

METHYLDOPA

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-12-05

71067 / 1 View Details

Active Ingredient

METHYLDOPA

Application Number

71067

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-12-05

Regulatory Status

Discontinued

1986

05 Dec

Discontinued Application: 71105

Drug Name

METHYLDOPA

Product Number

1

Dosage Form

-

Strength

125MG

Approval Date

1986-12-05

71105 / 1 View Details

Active Ingredient

METHYLDOPA

Application Number

71105

Product Number

1

Dosage Form

-

Strength

125MG

Approval Date

1986-12-05

Regulatory Status

Discontinued

1986

05 Dec

Discontinued Application: 71106

Drug Name

METHYLDOPA

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-12-05

71106 / 1 View Details

Active Ingredient

METHYLDOPA

Application Number

71106

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-12-05

Regulatory Status

Discontinued

1988

08 Apr

Discontinued Application: 71819

Drug Name

METHYLDOPA AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

15MG;250MG

Approval Date

1988-04-08

71819 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE; METHYLDOPA

Application Number

71819

Product Number

1

Dosage Form

-

Strength

15MG;250MG

Approval Date

1988-04-08

Regulatory Status

Discontinued

1988

08 Apr

Discontinued Application: 71820

Drug Name

METHYLDOPA AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;250MG

Approval Date

1988-04-08

71820 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE; METHYLDOPA

Application Number

71820

Product Number

1

Dosage Form

-

Strength

25MG;250MG

Approval Date

1988-04-08

Regulatory Status

Discontinued

1988

08 Apr

Discontinued Application: 71821

Drug Name

METHYLDOPA AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

30MG;500MG

Approval Date

1988-04-08

71821 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE; METHYLDOPA

Application Number

71821

Product Number

1

Dosage Form

-

Strength

30MG;500MG

Approval Date

1988-04-08

Regulatory Status

Discontinued

1988

08 Apr

Discontinued Application: 71822

Drug Name

METHYLDOPA AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

50MG;500MG

Approval Date

1988-04-08

71822 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE; METHYLDOPA

Application Number

71822

Product Number

1

Dosage Form

-

Strength

50MG;500MG

Approval Date

1988-04-08

Regulatory Status

Discontinued

1987

10 Jul

Discontinued Application: 70819

Drug Name

METOCLOPRAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

1987-07-10

70819 / 1 View Details

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

70819

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

1987-07-10

Regulatory Status

Discontinued

1993

30 Jun

Discontinued Application: 71315

Drug Name

METOCLOPRAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

1993-06-30

71315 / 1 View Details

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

71315

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

1993-06-30

Regulatory Status

Discontinued

1994

30 Sep

Discontinued Application: 74143

Drug Name

METOPROLOL TARTRATE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1994-09-30

74143 / 1 View Details

Active Ingredient

METOPROLOL TARTRATE

Application Number

74143

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1994-09-30

Regulatory Status

Discontinued

1994

30 Sep

Discontinued Application: 74143

Drug Name

METOPROLOL TARTRATE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1994-09-30

74143 / 2 View Details

Active Ingredient

METOPROLOL TARTRATE

Application Number

74143

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1994-09-30

Regulatory Status

Discontinued

1995

04 Jan

Discontinued Application: 74136

Drug Name

MICONAZOLE NITRATE

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1995-01-04

74136 / 1 View Details

Active Ingredient

MICONAZOLE NITRATE

Application Number

74136

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1995-01-04

Regulatory Status

Discontinued

1996

05 Apr

Discontinued Application: 74589

Drug Name

MINOXIDIL (FOR MEN)

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1996-04-05

74589 / 1 View Details

Active Ingredient

MINOXIDIL

Application Number

74589

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1996-04-05

Regulatory Status

Discontinued

1985

20 Sep

Discontinued Application: 61954

Drug Name

MYCO-TRIACET II

Product Number

2

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-09-20

61954 / 2 View Details

Active Ingredient

NYSTATIN; TRIAMCINOLONE ACETONIDE

Application Number

61954

Product Number

2

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-09-20

Regulatory Status

Discontinued

1985

26 Nov

Discontinued Application: 62045

Drug Name

MYCO-TRIACET II

Product Number

2

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-11-26

62045 / 2 View Details

Active Ingredient

NYSTATIN; TRIAMCINOLONE ACETONIDE

Application Number

62045

Product Number

2

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-11-26

Regulatory Status

Discontinued

1993

21 Dec

Discontinued Application: 74129

Drug Name

NAPROXEN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1993-12-21

74129 / 1 View Details

Active Ingredient

NAPROXEN

Application Number

74129

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1993-12-21

Regulatory Status

Discontinued

1993

21 Dec

Discontinued Application: 74129

Drug Name

NAPROXEN

Product Number

2

Dosage Form

-

Strength

375MG

Approval Date

1993-12-21

74129 / 2 View Details

Active Ingredient

NAPROXEN

Application Number

74129

Product Number

2

Dosage Form

-

Strength

375MG

Approval Date

1993-12-21

Regulatory Status

Discontinued

1993

21 Dec

Discontinued Application: 74129

Drug Name

NAPROXEN

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1993-12-21

74129 / 3 View Details

Active Ingredient

NAPROXEN

Application Number

74129

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1993-12-21

Regulatory Status

Discontinued

1996

11 Apr

Discontinued Application: 74216

Drug Name

NAPROXEN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1996-04-11

74216 / 1 View Details

Active Ingredient

NAPROXEN

Application Number

74216

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1996-04-11

Regulatory Status

Discontinued

1996

11 Apr

Discontinued Application: 74216

Drug Name

NAPROXEN

Product Number

2

Dosage Form

-

Strength

375MG

Approval Date

1996-04-11

74216 / 2 View Details

Active Ingredient

NAPROXEN

Application Number

74216

Product Number

2

Dosage Form

-

Strength

375MG

Approval Date

1996-04-11

Regulatory Status

Discontinued

1996

11 Apr

Discontinued Application: 74216

Drug Name

NAPROXEN

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1996-04-11

74216 / 3 View Details

Active Ingredient

NAPROXEN

Application Number

74216

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1996-04-11

Regulatory Status

Discontinued

1993

21 Dec

Discontinued Application: 74142

Drug Name

NAPROXEN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1993-12-21

74142 / 1 View Details

Active Ingredient

NAPROXEN SODIUM

Application Number

74142

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1993-12-21

Regulatory Status

Discontinued

1993

21 Dec

Discontinued Application: 74142

Drug Name

NAPROXEN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1993-12-21

74142 / 2 View Details

Active Ingredient

NAPROXEN SODIUM

Application Number

74142

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1993-12-21

Regulatory Status

Discontinued

1993

21 Dec

Discontinued Application: 74198

Drug Name

NAPROXEN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1993-12-21

74198 / 1 View Details

Active Ingredient

NAPROXEN SODIUM

Application Number

74198

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1993-12-21

Regulatory Status

Discontinued

1993

21 Dec

Discontinued Application: 74198

Drug Name

NAPROXEN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1993-12-21

74198 / 2 View Details

Active Ingredient

NAPROXEN SODIUM

Application Number

74198

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1993-12-21

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 7794

Drug Name

NEOTHYLLINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

7794 / 1 View Details

Active Ingredient

DYPHYLLINE

Application Number

7794

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 7794

Drug Name

NEOTHYLLINE

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

7794 / 2 View Details

Active Ingredient

DYPHYLLINE

Application Number

7794

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 7794

Drug Name

NEOTHYLLINE

Product Number

3

Dosage Form

-

Strength

160MG/15ML

Approval Date

1982-01-01

7794 / 3 View Details

Active Ingredient

DYPHYLLINE

Application Number

7794

Product Number

3

Dosage Form

-

Strength

160MG/15ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 9088

Drug Name

NEOTHYLLINE

Product Number

1

Dosage Form

-

Strength

250MG/ML

Approval Date

1982-01-01

9088 / 1 View Details

Active Ingredient

DYPHYLLINE

Application Number

9088

Product Number

1

Dosage Form

-

Strength

250MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1992

19 Feb

Discontinued Application: 72651

Drug Name

NIFEDIPINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1992-02-19

72651 / 1 View Details

Active Ingredient

NIFEDIPINE

Application Number

72651

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1992-02-19

Regulatory Status

Discontinued

1996

11 Apr

Discontinued Application: 73667

Drug Name

NORTRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1996-04-11

73667 / 1 View Details

Active Ingredient

NORTRIPTYLINE HYDROCHLORIDE

Application Number

73667

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1996-04-11

Regulatory Status

Discontinued

1996

11 Apr

Discontinued Application: 73667

Drug Name

NORTRIPTYLINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1996-04-11

73667 / 2 View Details

Active Ingredient

NORTRIPTYLINE HYDROCHLORIDE

Application Number

73667

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1996-04-11

Regulatory Status

Discontinued

1996

11 Apr

Discontinued Application: 73667

Drug Name

NORTRIPTYLINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1996-04-11

73667 / 3 View Details

Active Ingredient

NORTRIPTYLINE HYDROCHLORIDE

Application Number

73667

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1996-04-11

Regulatory Status

Discontinued

1996

11 Apr

Discontinued Application: 73667

Drug Name

NORTRIPTYLINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1996-04-11

73667 / 4 View Details

Active Ingredient

NORTRIPTYLINE HYDROCHLORIDE

Application Number

73667

Product Number

4

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1996-04-11

Regulatory Status

Discontinued

1983

23 Dec

Discontinued Application: 62502

Drug Name

NYSTATIN

Product Number

1

Dosage Form

-

Strength

100,000 UNITS

Approval Date

1983-12-23

62502 / 1 View Details

Active Ingredient

NYSTATIN

Application Number

62502

Product Number

1

Dosage Form

-

Strength

100,000 UNITS

Approval Date

1983-12-23

Regulatory Status

Discontinued

1987

18 Jun

Discontinued Application: 62670

Drug Name

NYSTATIN

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/ML

Approval Date

1987-06-18

62670 / 1 View Details

Active Ingredient

NYSTATIN

Application Number

62670

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/ML

Approval Date

1987-06-18

Regulatory Status

Discontinued

2007

25 Jun

Discontinued Application: 76810

Drug Name

ONDANSETRON

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2007-06-25

76810 / 1 View Details

Active Ingredient

ONDANSETRON

Application Number

76810

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2007-06-25

Regulatory Status

Discontinued

2007

25 Jun

Discontinued Application: 76810

Drug Name

ONDANSETRON

Product Number

2

Dosage Form

-

Strength

8MG

Approval Date

2007-06-25

76810 / 2 View Details

Active Ingredient

ONDANSETRON

Application Number

76810

Product Number

2

Dosage Form

-

Strength

8MG

Approval Date

2007-06-25

Regulatory Status

Discontinued

2007

25 Jun

Discontinued Application: 76252

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2007-06-25

76252 / 1 View Details

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

76252

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2007-06-25

Regulatory Status

Discontinued

2007

25 Jun

Discontinued Application: 76252

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2007-06-25

76252 / 2 View Details

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

76252

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2007-06-25

Regulatory Status

Discontinued

2007

25 Jun

Discontinued Application: 76252

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 24MG BASE

Approval Date

2007-06-25

76252 / 3 View Details

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

76252

Product Number

3

Dosage Form

-

Strength

EQ 24MG BASE

Approval Date

2007-06-25

Regulatory Status

Discontinued

2006

22 Nov

Discontinued Application: 76876

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2006-11-22

76876 / 1 View Details

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

76876

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2006-11-22

Regulatory Status

Discontinued

2006

22 Nov

Discontinued Application: 76759

Drug Name

ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2006-11-22

76759 / 1 View Details

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

76759

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2006-11-22

Regulatory Status

Discontinued

1984

31 Jul

Discontinued Application: 17473

Drug Name

ORAP

Product Number

1

Dosage Form

-

Strength

2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-07-31

17473 / 1 View Details

Active Ingredient

PIMOZIDE

Application Number

17473

Product Number

1

Dosage Form

-

Strength

2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-07-31

Regulatory Status

Discontinued

1997

27 Aug

Discontinued Application: 17473

Drug Name

ORAP

Product Number

3

Dosage Form

-

Strength

1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1997-08-27

17473 / 3 View Details

Active Ingredient

PIMOZIDE

Application Number

17473

Product Number

3

Dosage Form

-

Strength

1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1997-08-27

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62252

Drug Name

OXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

62252 / 1 View Details

Active Ingredient

OXACILLIN SODIUM

Application Number

62252

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

2002

03 Jul

Discontinued Application: 75849

Drug Name

OXAPROZIN

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2002-07-03

75849 / 1 View Details

Active Ingredient

OXAPROZIN

Application Number

75849

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2002-07-03

Regulatory Status

Discontinued

2007

02 Aug

Discontinued Application: 77056

Drug Name

PANTOPRAZOLE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2007-08-02

77056 / 1 View Details

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

77056

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2007-08-02

Regulatory Status

Discontinued

2007

02 Aug

Discontinued Application: 77056

Drug Name

PANTOPRAZOLE SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2007-08-02

77056 / 2 View Details

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

77056

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2007-08-02

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 60307

Drug Name

PENICILLIN

Product Number

2

Dosage Form

-

Strength

200,000 UNITS/5ML

Approval Date

1982-01-01

60307 / 2 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60307

Product Number

2

Dosage Form

-

Strength

200,000 UNITS/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 60307

Drug Name

PENICILLIN

Product Number

4

Dosage Form

-

Strength

400,000 UNITS/5ML

Approval Date

1982-01-01

60307 / 4 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60307

Product Number

4

Dosage Form

-

Strength

400,000 UNITS/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 60306

Drug Name

PENICILLIN G POTASSIUM

Product Number

1

Dosage Form

-

Strength

200,000 UNITS

Approval Date

1982-01-01

60306 / 1 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60306

Product Number

1

Dosage Form

-

Strength

200,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 60306

Drug Name

PENICILLIN G POTASSIUM

Product Number

2

Dosage Form

-

Strength

250,000 UNITS

Approval Date

1982-01-01

60306 / 2 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60306

Product Number

2

Dosage Form

-

Strength

250,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 60306

Drug Name

PENICILLIN G POTASSIUM

Product Number

3

Dosage Form

-

Strength

400,000 UNITS

Approval Date

1982-01-01

60306 / 3 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60306

Product Number

3

Dosage Form

-

Strength

400,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 60306

Drug Name

PENICILLIN G POTASSIUM

Product Number

4

Dosage Form

-

Strength

500,000 UNITS

Approval Date

1982-01-01

60306 / 4 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60306

Product Number

4

Dosage Form

-

Strength

500,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 60307

Drug Name

PENICILLIN-2

Product Number

3

Dosage Form

-

Strength

250,000 UNITS/5ML

Approval Date

1982-01-01

60307 / 3 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60307

Product Number

3

Dosage Form

-

Strength

250,000 UNITS/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86911

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1982-01-01

86911 / 1 View Details

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

86911

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 87126

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1982-01-01

87126 / 1 View Details

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

87126

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985

01 Nov

Discontinued Application: 87777

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1985-11-01

87777 / 1 View Details

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

87777

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1985-11-01

Regulatory Status

Discontinued

1984

04 Apr

Discontinued Application: 88612

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1984-04-04

88612 / 1 View Details

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

88612

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1984-04-04

Regulatory Status

Discontinued

1984

09 Apr

Discontinued Application: 88613

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1984-04-09

88613 / 1 View Details

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

88613

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1984-04-09

Regulatory Status

Discontinued

1984

09 Apr

Discontinued Application: 88614

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1984-04-09

88614 / 1 View Details

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

88614

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1984-04-09

Regulatory Status

Discontinued

1994

28 Jan

Discontinued Application: 73637

Drug Name

PIROXICAM

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1994-01-28

73637 / 1 View Details

Active Ingredient

PIROXICAM

Application Number

73637

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1994-01-28

Regulatory Status

Discontinued

1994

28 Jan

Discontinued Application: 73638

Drug Name

PIROXICAM

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1994-01-28

73638 / 1 View Details

Active Ingredient

PIROXICAM

Application Number

73638

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1994-01-28

Regulatory Status

Discontinued

1996

26 Apr

Discontinued Application: 73531

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

8MEQ

Approval Date

1996-04-26

73531 / 1 View Details

Active Ingredient

POTASSIUM CHLORIDE

Application Number

73531

Product Number

1

Dosage Form

-

Strength

8MEQ

Approval Date

1996-04-26

Regulatory Status

Discontinued

1996

26 Apr

Discontinued Application: 73532

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

10MEQ

Approval Date

1996-04-26

73532 / 1 View Details

Active Ingredient

POTASSIUM CHLORIDE

Application Number

73532

Product Number

1

Dosage Form

-

Strength

10MEQ

Approval Date

1996-04-26

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80398

Drug Name

PREDNISOLONE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

80398 / 1 View Details

Active Ingredient

PREDNISOLONE

Application Number

80398

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80397

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

80397 / 1 View Details

Active Ingredient

PREDNISONE

Application Number

80397

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985

10 Sep

Discontinued Application: 89109

Drug Name

PROMETHAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-09-10

89109 / 1 View Details

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

89109

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-09-10

Regulatory Status

Discontinued

1985

12 Jun

Discontinued Application: 70107

Drug Name

PROPACET 100

Product Number

1

Dosage Form

-

Strength

650MG;100MG

Approval Date

1985-06-12

70107 / 1 View Details

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

70107

Product Number

1

Dosage Form

-

Strength

650MG;100MG

Approval Date

1985-06-12

Regulatory Status

Discontinued

1985

29 Mar

Discontinued Application: 89025

Drug Name

PROPOXYPHENE COMPOUND 65

Product Number

1

Dosage Form

-

Strength

389MG;32.4MG;65MG

Approval Date

1985-03-29

89025 / 1 View Details

Active Ingredient

ASPIRIN; CAFFEINE; PROPOXYPHENE HYDROCHLORIDE

Application Number

89025

Product Number

1

Dosage Form

-

Strength

389MG;32.4MG;65MG

Approval Date

1985-03-29

Regulatory Status

Discontinued

1984

22 Oct

Discontinued Application: 88615

Drug Name

PROPOXYPHENE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1984-10-22

88615 / 1 View Details

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

88615

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1984-10-22

Regulatory Status

Discontinued

1986

03 Jan

Discontinued Application: 70732

Drug Name

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG;100MG

Approval Date

1986-01-03

70732 / 1 View Details

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

70732

Product Number

1

Dosage Form

-

Strength

650MG;100MG

Approval Date

1986-01-03

Regulatory Status

Discontinued

1994

19 Dec

Discontinued Application: 74119

Drug Name

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG;100MG

Approval Date

1994-12-19

74119 / 1 View Details

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

74119

Product Number

1

Dosage Form

-

Strength

650MG;100MG

Approval Date

1994-12-19

Regulatory Status

Discontinued

1987

07 Oct

Discontinued Application: 70232

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1987-10-07

70232 / 1 View Details

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70232

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1987-10-07

Regulatory Status

Discontinued

1986

23 Jun

Discontinued Application: 70233

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1986-06-23

70233 / 1 View Details

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70233

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1986-06-23

Regulatory Status

Discontinued

1986

23 Jun

Discontinued Application: 70234

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1986-06-23

70234 / 1 View Details

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70234

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1986-06-23

Regulatory Status

Discontinued

2003

31 Oct

Discontinued Application: 75557

Drug Name

RANITIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2003-10-31

75557 / 1 View Details

Active Ingredient

RANITIDINE HYDROCHLORIDE

Application Number

75557

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2003-10-31

Regulatory Status

Discontinued

2003

31 Oct

Discontinued Application: 75557

Drug Name

RANITIDINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 300MG BASE

Approval Date

2003-10-31

75557 / 2 View Details

Active Ingredient

RANITIDINE HYDROCHLORIDE

Application Number

75557

Product Number

2

Dosage Form

-

Strength

EQ 300MG BASE

Approval Date

2003-10-31

Regulatory Status

Discontinued

1985

07 Mar

Discontinued Application: 89019

Drug Name

RESERPINE

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

1985-03-07

89019 / 1 View Details

Active Ingredient

RESERPINE

Application Number

89019

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

1985-03-07

Regulatory Status

Discontinued

1985

07 Mar

Discontinued Application: 89020

Drug Name

RESERPINE

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1985-03-07

89020 / 1 View Details

Active Ingredient

RESERPINE

Application Number

89020

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1985-03-07

Regulatory Status

Discontinued

2004

04 Oct

Discontinued Application: 76277

Drug Name

RIBAVIRIN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2004-10-04

76277 / 1 View Details

Active Ingredient

RIBAVIRIN

Application Number

76277

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2004-10-04

Regulatory Status

Discontinued

2014

07 May

Discontinued Application: 77337

Drug Name

ROSIGLITAZONE MALEATE AND METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG;EQ 2MG BASE

Approval Date

2014-05-07

77337 / 1 View Details

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Application Number

77337

Product Number

1

Dosage Form

-

Strength

500MG;EQ 2MG BASE

Approval Date

2014-05-07

Regulatory Status

Discontinued

2014

07 May

Discontinued Application: 77337

Drug Name

ROSIGLITAZONE MALEATE AND METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

500MG;EQ 4MG BASE

Approval Date

2014-05-07

77337 / 2 View Details

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Application Number

77337

Product Number

2

Dosage Form

-

Strength

500MG;EQ 4MG BASE

Approval Date

2014-05-07

Regulatory Status

Discontinued

2014

07 May

Discontinued Application: 77337

Drug Name

ROSIGLITAZONE MALEATE AND METFORMIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

1GM;EQ 2MG BASE

Approval Date

2014-05-07

77337 / 3 View Details

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Application Number

77337

Product Number

3

Dosage Form

-

Strength

1GM;EQ 2MG BASE

Approval Date

2014-05-07

Regulatory Status

Discontinued

2014

07 May

Discontinued Application: 77337

Drug Name

ROSIGLITAZONE MALEATE AND METFORMIN HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

1GM;EQ 4MG BASE

Approval Date

2014-05-07

77337 / 4 View Details

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Application Number

77337

Product Number

4

Dosage Form

-

Strength

1GM;EQ 4MG BASE

Approval Date

2014-05-07

Regulatory Status

Discontinued

2017

19 May

Discontinued Application: 77337

Drug Name

ROSIGLITAZONE MALEATE AND METFORMIN HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

500MG;EQ 1MG BASE

Approval Date

2017-05-19

77337 / 5 View Details

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Application Number

77337

Product Number

5

Dosage Form

-

Strength

500MG;EQ 1MG BASE

Approval Date

2017-05-19

Regulatory Status

Discontinued

2004

26 Jul

Discontinued Application: 76883

Drug Name

SOTALOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

2004-07-26

76883 / 1 View Details

Active Ingredient

SOTALOL HYDROCHLORIDE

Application Number

76883

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

2004-07-26

Regulatory Status

Discontinued

2004

26 Jul

Discontinued Application: 76883

Drug Name

SOTALOL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

120MG

Approval Date

2004-07-26

76883 / 2 View Details

Active Ingredient

SOTALOL HYDROCHLORIDE

Application Number

76883

Product Number

2

Dosage Form

-

Strength

120MG

Approval Date

2004-07-26

Regulatory Status

Discontinued

2004

26 Jul

Discontinued Application: 76883

Drug Name

SOTALOL HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

160MG

Approval Date

2004-07-26

76883 / 3 View Details

Active Ingredient

SOTALOL HYDROCHLORIDE

Application Number

76883

Product Number

3

Dosage Form

-

Strength

160MG

Approval Date

2004-07-26

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85507

Drug Name

STATOBEX

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

85507 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

85507

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86013

Drug Name

STATOBEX

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

86013 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

86013

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85095

Drug Name

STATOBEX-G

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

85095 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

85095

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18242

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

1

Dosage Form

-

Strength

400MG;80MG

Approval Date

1982-01-01

18242 / 1 View Details

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

18242

Product Number

1

Dosage Form

-

Strength

400MG;80MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18242

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

2

Dosage Form

-

Strength

800MG;160MG

Approval Date

1982-01-01

18242 / 2 View Details

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

18242

Product Number

2

Dosage Form

-

Strength

800MG;160MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983

28 Jan

Discontinued Application: 18812

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

1

Dosage Form

-

Strength

200MG/5ML;40MG/5ML

Approval Date

1983-01-28

18812 / 1 View Details

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

18812

Product Number

1

Dosage Form

-

Strength

200MG/5ML;40MG/5ML

Approval Date

1983-01-28

Regulatory Status

Discontinued

1983

10 Jun

Discontinued Application: 18812

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

2

Dosage Form

-

Strength

200MG/5ML;40MG/5ML

Approval Date

1983-06-10

18812 / 2 View Details

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

18812

Product Number

2

Dosage Form

-

Strength

200MG/5ML;40MG/5ML

Approval Date

1983-06-10

Regulatory Status

Discontinued

2009

09 Feb

Discontinued Application: 76840

Drug Name

SUMATRIPTAN SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2009-02-09

76840 / 1 View Details

Active Ingredient

SUMATRIPTAN SUCCINATE

Application Number

76840

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2009-02-09

Regulatory Status

Discontinued

2009

09 Feb

Discontinued Application: 76840

Drug Name

SUMATRIPTAN SUCCINATE

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2009-02-09

76840 / 2 View Details

Active Ingredient

SUMATRIPTAN SUCCINATE

Application Number

76840

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2009-02-09

Regulatory Status

Discontinued

2009

09 Feb

Discontinued Application: 76840

Drug Name

SUMATRIPTAN SUCCINATE

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2009-02-09

76840 / 3 View Details

Active Ingredient

SUMATRIPTAN SUCCINATE

Application Number

76840

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2009-02-09

Regulatory Status

Discontinued

2003

28 Apr

Discontinued Application: 74504

Drug Name

TAMOXIFEN CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2003-04-28

74504 / 1 View Details

Active Ingredient

TAMOXIFEN CITRATE

Application Number

74504

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2003-04-28

Regulatory Status

Discontinued

2003

28 Apr

Discontinued Application: 74504

Drug Name

TAMOXIFEN CITRATE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2003-04-28

74504 / 2 View Details

Active Ingredient

TAMOXIFEN CITRATE

Application Number

74504

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2003-04-28

Regulatory Status

Discontinued

2000

18 May

Discontinued Application: 74446

Drug Name

TERAZOSIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2000-05-18

74446 / 1 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

74446

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2000-05-18

Regulatory Status

Discontinued

2000

18 May

Discontinued Application: 74446

Drug Name

TERAZOSIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2000-05-18

74446 / 2 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

74446

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2000-05-18

Regulatory Status

Discontinued

2000

18 May

Discontinued Application: 74446

Drug Name

TERAZOSIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2000-05-18

74446 / 3 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

74446

Product Number

3

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2000-05-18

Regulatory Status

Discontinued

2000

18 May

Discontinued Application: 74446

Drug Name

TERAZOSIN HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2000-05-18

74446 / 4 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

74446

Product Number

4

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2000-05-18

Regulatory Status

Discontinued

1987

22 Jun

Discontinued Application: 71184

Drug Name

THIOTHIXENE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

1987-06-22

71184 / 1 View Details

Active Ingredient

THIOTHIXENE HYDROCHLORIDE

Application Number

71184

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

1987-06-22

Regulatory Status

Discontinued

1999

20 Aug

Discontinued Application: 75149

Drug Name

TICLOPIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1999-08-20

75149 / 1 View Details

Active Ingredient

TICLOPIDINE HYDROCHLORIDE

Application Number

75149

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1999-08-20

Regulatory Status

Discontinued

1993

16 Jun

Discontinued Application: 72648

Drug Name

TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1993-06-16

72648 / 1 View Details

Active Ingredient

TIMOLOL MALEATE

Application Number

72648

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1993-06-16

Regulatory Status

Discontinued

1993

16 Jun

Discontinued Application: 72649

Drug Name

TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1993-06-16

72649 / 1 View Details

Active Ingredient

TIMOLOL MALEATE

Application Number

72649

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1993-06-16

Regulatory Status

Discontinued

1993

16 Jun

Discontinued Application: 72650

Drug Name

TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1993-06-16

72650 / 1 View Details

Active Ingredient

TIMOLOL MALEATE

Application Number

72650

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1993-06-16

Regulatory Status

Discontinued

2009

27 Mar

Discontinued Application: 76317

Drug Name

TOPIRAMATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2009-03-27

76317 / 1 View Details

Active Ingredient

TOPIRAMATE

Application Number

76317

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2009-03-27

Regulatory Status

Discontinued

2009

27 Mar

Discontinued Application: 76317

Drug Name

TOPIRAMATE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2009-03-27

76317 / 2 View Details

Active Ingredient

TOPIRAMATE

Application Number

76317

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2009-03-27

Regulatory Status

Discontinued

2009

27 Mar

Discontinued Application: 76317

Drug Name

TOPIRAMATE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2009-03-27

76317 / 3 View Details

Active Ingredient

TOPIRAMATE

Application Number

76317

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2009-03-27

Regulatory Status

Discontinued

2009

27 Mar

Discontinued Application: 76317

Drug Name

TOPIRAMATE

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2009-03-27

76317 / 4 View Details

Active Ingredient

TOPIRAMATE

Application Number

76317

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2009-03-27

Regulatory Status

Discontinued

2009

17 Apr

Discontinued Application: 76575

Drug Name

TOPIRAMATE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2009-04-17

76575 / 1 View Details

Active Ingredient

TOPIRAMATE

Application Number

76575

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2009-04-17

Regulatory Status

Discontinued

2009

17 Apr

Discontinued Application: 76575

Drug Name

TOPIRAMATE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2009-04-17

76575 / 2 View Details

Active Ingredient

TOPIRAMATE

Application Number

76575

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2009-04-17

Regulatory Status

Discontinued

2002

14 May

Discontinued Application: 76110

Drug Name

TORSEMIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2002-05-14

76110 / 1 View Details

Active Ingredient

TORSEMIDE

Application Number

76110

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2002-05-14

Regulatory Status

Discontinued

2002

14 May

Discontinued Application: 76110

Drug Name

TORSEMIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2002-05-14

76110 / 2 View Details

Active Ingredient

TORSEMIDE

Application Number

76110

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2002-05-14

Regulatory Status

Discontinued

2002

14 May

Discontinued Application: 76110

Drug Name

TORSEMIDE

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

2002-05-14

76110 / 3 View Details

Active Ingredient

TORSEMIDE

Application Number

76110

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

2002-05-14

Regulatory Status

Discontinued

2002

14 May

Discontinued Application: 76110

Drug Name

TORSEMIDE

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2002-05-14

76110 / 4 View Details

Active Ingredient

TORSEMIDE

Application Number

76110

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2002-05-14

Regulatory Status

Discontinued

1997

30 Apr

Discontinued Application: 74357

Drug Name

TRAZODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

1997-04-30

74357 / 1 View Details

Active Ingredient

TRAZODONE HYDROCHLORIDE

Application Number

74357

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

1997-04-30

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84908

Drug Name

TRIACET

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

84908 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

84908

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84908

Drug Name

TRIACET

Product Number

2

Dosage Form

-

Strength

0.1%

Approval Date

1982-01-01

84908 / 2 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

84908

Product Number

2

Dosage Form

-

Strength

0.1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84908

Drug Name

TRIACET

Product Number

3

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

84908 / 3 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

84908

Product Number

3

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84775

Drug Name

TRIAMCINOLONE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

84775 / 1 View Details

Active Ingredient

TRIAMCINOLONE

Application Number

84775

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987

18 Jun

Discontinued Application: 71259

Drug Name

TRIMETHOPRIM

Product Number

1

Dosage Form

-

Strength

200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-06-18

71259 / 1 View Details

Active Ingredient

TRIMETHOPRIM

Application Number

71259

Product Number

1

Dosage Form

-

Strength

200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-06-18

Regulatory Status

Discontinued

1984

17 May

Discontinued Application: 88630

Drug Name

TRIPHED

Product Number

1

Dosage Form

-

Strength

60MG;2.5MG

Approval Date

1984-05-17

88630 / 1 View Details

Active Ingredient

PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE

Application Number

88630

Product Number

1

Dosage Form

-

Strength

60MG;2.5MG

Approval Date

1984-05-17

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80921

Drug Name

VITAMIN A SOLUBILIZED

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

80921 / 1 View Details

Active Ingredient

VITAMIN A PALMITATE

Application Number

80921

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

2007

23 Apr

Discontinued Application: 76410

Drug Name

ZOLPIDEM TARTRATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2007-04-23

76410 / 1 View Details

Active Ingredient

ZOLPIDEM TARTRATE

Application Number

76410

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2007-04-23

Regulatory Status

Discontinued

2007

23 Apr

Discontinued Application: 76410

Drug Name

ZOLPIDEM TARTRATE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2007-04-23

76410 / 2 View Details

Active Ingredient

ZOLPIDEM TARTRATE

Application Number

76410

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2007-04-23

Regulatory Status

Discontinued

Assia Chemical Industries Ltd Discontinued
FDA Approved Drugs

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Assia Chemical Industries Ltd Discontinued FDA Approved Drugs