Bristol Myers Squibb Discontinued
FDA Approved Drugs

Bristol Myers Squibb Discontinued

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

Discontinued
  • Total Records 182
  • Latest Approval Date Jun 24, 2003
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
217
View
Unclassified
12
View
Discontinued
182
View
RX
23
View
Company Overview

Company

Bristol Myers Squibb Discontinued

Country

U.S.A

Website

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Company Snapshot

Bristol Myers Squibb Discontinued

430 E. 29th Street, 14th Floor, New York, NY 10016

U.S.A

www.bms.com/ View on Map
FDA Approved Drug Records ( 182 records )
1982
01 Jan
Discontinued Application: 86454

Drug Name

AMITID

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

86454 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86454

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86454

Drug Name

AMITID

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

86454 / 2

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86454

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86454

Drug Name

AMITID

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

86454 / 3

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86454

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86454

Drug Name

AMITID

Product Number

4

Dosage Form

-

Strength

75MG

Approval Date

1982-01-01

86454 / 4

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86454

Product Number

4

Dosage Form

-

Strength

75MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86454

Drug Name

AMITID

Product Number

5

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

86454 / 5

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86454

Product Number

5

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83266

Drug Name

AMNESTROGEN

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

1982-01-01

83266 / 1

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

83266

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83266

Drug Name

AMNESTROGEN

Product Number

2

Dosage Form

-

Strength

0.625MG

Approval Date

1982-01-01

83266 / 2

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

83266

Product Number

2

Dosage Form

-

Strength

0.625MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83266

Drug Name

AMNESTROGEN

Product Number

3

Dosage Form

-

Strength

1.25MG

Approval Date

1982-01-01

83266 / 3

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

83266

Product Number

3

Dosage Form

-

Strength

1.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83266

Drug Name

AMNESTROGEN

Product Number

4

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

83266 / 4

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

83266

Product Number

4

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989
24 May
Discontinued Application: 50632

Drug Name

AZACTAM IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1989-05-24

50632 / 1

Active Ingredient

AZTREONAM

Application Number

50632

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1989-05-24

Regulatory Status

Discontinued

1989
24 May
Discontinued Application: 50632

Drug Name

AZACTAM IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

20MG/ML

Approval Date

1989-05-24

50632 / 2

Active Ingredient

AZTREONAM

Application Number

50632

Product Number

2

Dosage Form

-

Strength

20MG/ML

Approval Date

1989-05-24

Regulatory Status

Discontinued

1989
24 May
Discontinued Application: 50632

Drug Name

AZACTAM IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

10MG/ML

Approval Date

1989-05-24

50632 / 3

Active Ingredient

AZTREONAM

Application Number

50632

Product Number

3

Dosage Form

-

Strength

10MG/ML

Approval Date

1989-05-24

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50443

Drug Name

BLENOXANE

Product Number

1

Dosage Form

-

Strength

EQ 15 UNITS BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50443 / 1

Active Ingredient

BLEOMYCIN SULFATE

Application Number

50443

Product Number

1

Dosage Form

-

Strength

EQ 15 UNITS BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1995
07 Sep
Discontinued Application: 50443

Drug Name

BLENOXANE

Product Number

2

Dosage Form

-

Strength

EQ 30 UNITS BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1995-09-07

50443 / 2

Active Ingredient

BLEOMYCIN SULFATE

Application Number

50443

Product Number

2

Dosage Form

-

Strength

EQ 30 UNITS BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1995-09-07

Regulatory Status

Discontinued

1986
29 Sep
Discontinued Application: 18731

Drug Name

BUSPAR

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1986-09-29

18731 / 1

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

18731

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1986-09-29

Regulatory Status

Discontinued

1986
29 Sep
Discontinued Application: 18731

Drug Name

BUSPAR

Product Number

2

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1986-09-29

18731 / 2

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

18731

Product Number

2

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1986-09-29

Regulatory Status

Discontinued

1996
22 Apr
Discontinued Application: 18731

Drug Name

BUSPAR

Product Number

3

Dosage Form

-

Strength

15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-04-22

18731 / 3

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

18731

Product Number

3

Dosage Form

-

Strength

15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-04-22

Regulatory Status

Discontinued

1996
22 Apr
Discontinued Application: 18731

Drug Name

BUSPAR

Product Number

4

Dosage Form

-

Strength

30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-04-22

18731 / 4

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

18731

Product Number

4

Dosage Form

-

Strength

30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-04-22

Regulatory Status

Discontinued

2000
20 Dec
Discontinued Application: 21190

Drug Name

BUSPAR

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2000-12-20

21190 / 1

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

21190

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2000-12-20

Regulatory Status

Discontinued

2000
20 Dec
Discontinued Application: 21190

Drug Name

BUSPAR

Product Number

2

Dosage Form

-

Strength

7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-12-20

21190 / 2

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

21190

Product Number

2

Dosage Form

-

Strength

7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-12-20

Regulatory Status

Discontinued

2000
20 Dec
Discontinued Application: 21190

Drug Name

BUSPAR

Product Number

3

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-12-20

21190 / 3

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

21190

Product Number

3

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-12-20

Regulatory Status

Discontinued

2000
20 Dec
Discontinued Application: 21190

Drug Name

BUSPAR

Product Number

4

Dosage Form

-

Strength

15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-12-20

21190 / 4

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

21190

Product Number

4

Dosage Form

-

Strength

15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-12-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17594

Drug Name

CAPITROL

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

17594 / 1

Active Ingredient

CHLOROXINE

Application Number

17594

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989
01 Feb
Discontinued Application: 62908

Drug Name

CLINDAMYCIN PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/ML

Approval Date

1989-02-01

62908 / 1

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

62908

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/ML

Approval Date

1989-02-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

5

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

9218 / 5

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

5

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

7

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

9218 / 7

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

7

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

12

Dosage Form

-

Strength

75MG/VIAL

Approval Date

1982-01-01

9218 / 12

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

12

Dosage Form

-

Strength

75MG/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

13

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

9218 / 13

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

13

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

16

Dosage Form

-

Strength

7.5MG

Approval Date

1982-01-01

9218 / 16

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

16

Dosage Form

-

Strength

7.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

18

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

9218 / 18

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

18

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

20

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1982-01-01

9218 / 20

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

20

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1990
01 Mar
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

22

Dosage Form

-

Strength

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

Approval Date

1990-03-01

9218 / 22

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

22

Dosage Form

-

Strength

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

Approval Date

1990-03-01

Regulatory Status

Discontinued

1993
24 Aug
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

23

Dosage Form

-

Strength

4MG

Approval Date

1993-08-24

9218 / 23

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

23

Dosage Form

-

Strength

4MG

Approval Date

1993-08-24

Regulatory Status

Discontinued

1995
07 Feb
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

24

Dosage Form

-

Strength

5MG/VIAL

Approval Date

1995-02-07

9218 / 24

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

24

Dosage Form

-

Strength

5MG/VIAL

Approval Date

1995-02-07

Regulatory Status

Discontinued

1996
18 Nov
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

25

Dosage Form

-

Strength

3MG

Approval Date

1996-11-18

9218 / 25

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

25

Dosage Form

-

Strength

3MG

Approval Date

1996-11-18

Regulatory Status

Discontinued

1996
18 Nov
Discontinued Application: 9218

Drug Name

COUMADIN

Product Number

26

Dosage Form

-

Strength

6MG

Approval Date

1996-11-18

9218 / 26

Active Ingredient

WARFARIN SODIUM

Application Number

9218

Product Number

26

Dosage Form

-

Strength

6MG

Approval Date

1996-11-18

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85020

Drug Name

DEAPRIL-ST

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

85020 / 2

Active Ingredient

ERGOLOID MESYLATES

Application Number

85020

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 10347

Drug Name

DELALUTIN

Product Number

2

Dosage Form

-

Strength

250MG/ML (250MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

10347 / 2

Active Ingredient

HYDROXYPROGESTERONE CAPROATE

Application Number

10347

Product Number

2

Dosage Form

-

Strength

250MG/ML (250MG/ML) **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: 10347

Drug Name

DELALUTIN

Product Number

4

Dosage Form

-

Strength

125MG/ML (125MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

10347 / 4

Active Ingredient

HYDROXYPROGESTERONE CAPROATE

Application Number

10347

Product Number

4

Dosage Form

-

Strength

125MG/ML (125MG/ML) **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: 16911

Drug Name

DELALUTIN

Product Number

1

Dosage Form

-

Strength

125MG/ML (125MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

16911 / 1

Active Ingredient

HYDROXYPROGESTERONE CAPROATE

Application Number

16911

Product Number

1

Dosage Form

-

Strength

125MG/ML (125MG/ML) **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: 16911

Drug Name

DELALUTIN

Product Number

2

Dosage Form

-

Strength

250MG/ML (250MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

16911 / 2

Active Ingredient

HYDROXYPROGESTERONE CAPROATE

Application Number

16911

Product Number

2

Dosage Form

-

Strength

250MG/ML (250MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993
30 Jun
Discontinued Application: 81295

Drug Name

ESTRACE

Product Number

1

Dosage Form

-

Strength

0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-06-30

81295 / 1

Active Ingredient

ESTRADIOL

Application Number

81295

Product Number

1

Dosage Form

-

Strength

0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-06-30

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84499

Drug Name

ESTRACE

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

84499 / 1

Active Ingredient

ESTRADIOL

Application Number

84499

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84500

Drug Name

ESTRACE

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

84500 / 1

Active Ingredient

ESTRADIOL

Application Number

84500

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61605

Drug Name

ETHRIL 250

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

61605 / 1

Active Ingredient

ERYTHROMYCIN STEARATE

Application Number

61605

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61605

Drug Name

ETHRIL 500

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

61605 / 2

Active Ingredient

ERYTHROMYCIN STEARATE

Application Number

61605

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1998
27 Feb
Discontinued Application: 20906

Drug Name

ETOPOPHOS PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1998-02-27

20906 / 1

Active Ingredient

ETOPOSIDE PHOSPHATE

Application Number

20906

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1998-02-27

Regulatory Status

Discontinued

1998
27 Feb
Discontinued Application: 20906

Drug Name

ETOPOPHOS PRESERVATIVE FREE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1998-02-27

20906 / 2

Active Ingredient

ETOPOSIDE PHOSPHATE

Application Number

20906

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1998-02-27

Regulatory Status

Discontinued

1982
08 Apr
Discontinued Application: 87136

Drug Name

FLEXICORT

Product Number

1

Dosage Form

-

Strength

2.5%

Approval Date

1982-04-08

87136 / 1

Active Ingredient

HYDROCORTISONE

Application Number

87136

Product Number

1

Dosage Form

-

Strength

2.5%

Approval Date

1982-04-08

Regulatory Status

Discontinued

1982
08 Apr
Discontinued Application: 87136

Drug Name

FLEXICORT

Product Number

2

Dosage Form

-

Strength

1%

Approval Date

1982-04-08

87136 / 2

Active Ingredient

HYDROCORTISONE

Application Number

87136

Product Number

2

Dosage Form

-

Strength

1%

Approval Date

1982-04-08

Regulatory Status

Discontinued

1982
08 Apr
Discontinued Application: 87136

Drug Name

FLEXICORT

Product Number

3

Dosage Form

-

Strength

0.5%

Approval Date

1982-04-08

87136 / 3

Active Ingredient

HYDROCORTISONE

Application Number

87136

Product Number

3

Dosage Form

-

Strength

0.5%

Approval Date

1982-04-08

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50341

Drug Name

FUNGIZONE

Product Number

3

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

50341 / 3

Active Ingredient

AMPHOTERICIN B

Application Number

50341

Product Number

3

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17907

Drug Name

GLUCOSCAN

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1982-01-01

17907 / 1

Active Ingredient

TECHNETIUM TC-99M GLUCEPTATE KIT

Application Number

17907

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1982-01-01

Regulatory Status

Discontinued

2000
31 Jul
Discontinued Application: 21178

Drug Name

GLUCOVANCE

Product Number

1

Dosage Form

-

Strength

1.25MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-07-31

21178 / 1

Active Ingredient

GLYBURIDE; METFORMIN HYDROCHLORIDE

Application Number

21178

Product Number

1

Dosage Form

-

Strength

1.25MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-07-31

Regulatory Status

Discontinued

2000
31 Jul
Discontinued Application: 21178

Drug Name

GLUCOVANCE

Product Number

2

Dosage Form

-

Strength

2.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-07-31

21178 / 2

Active Ingredient

GLYBURIDE; METFORMIN HYDROCHLORIDE

Application Number

21178

Product Number

2

Dosage Form

-

Strength

2.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-07-31

Regulatory Status

Discontinued

2000
31 Jul
Discontinued Application: 21178

Drug Name

GLUCOVANCE

Product Number

3

Dosage Form

-

Strength

5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-07-31

21178 / 3

Active Ingredient

GLYBURIDE; METFORMIN HYDROCHLORIDE

Application Number

21178

Product Number

3

Dosage Form

-

Strength

5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-07-31

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17818

Drug Name

HALOG

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

17818 / 1

Active Ingredient

HALCINONIDE

Application Number

17818

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18125

Drug Name

HALOG

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

18125 / 1

Active Ingredient

HALCINONIDE

Application Number

18125

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16942

Drug Name

HALOTEX

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

16942 / 1

Active Ingredient

HALOPROGIN

Application Number

16942

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16943

Drug Name

HALOTEX

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

16943 / 1

Active Ingredient

HALOPROGIN

Application Number

16943

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16979

Drug Name

MEGACE

Product Number

1

Dosage Form

-

Strength

20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

16979 / 1

Active Ingredient

MEGESTROL ACETATE

Application Number

16979

Product Number

1

Dosage Form

-

Strength

20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16979

Drug Name

MEGACE

Product Number

2

Dosage Form

-

Strength

40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

16979 / 2

Active Ingredient

MEGESTROL ACETATE

Application Number

16979

Product Number

2

Dosage Form

-

Strength

40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993
10 Sep
Discontinued Application: 20264

Drug Name

MEGACE

Product Number

1

Dosage Form

-

Strength

40MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-09-10

20264 / 1

Active Ingredient

MEGESTROL ACETATE

Application Number

20264

Product Number

1

Dosage Form

-

Strength

40MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-09-10

Regulatory Status

Discontinued

2002
21 Oct
Discontinued Application: 21460

Drug Name

METAGLIP

Product Number

1

Dosage Form

-

Strength

2.5MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-21

21460 / 1

Active Ingredient

GLIPIZIDE; METFORMIN HYDROCHLORIDE

Application Number

21460

Product Number

1

Dosage Form

-

Strength

2.5MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-21

Regulatory Status

Discontinued

2002
21 Oct
Discontinued Application: 21460

Drug Name

METAGLIP

Product Number

2

Dosage Form

-

Strength

2.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-21

21460 / 2

Active Ingredient

GLIPIZIDE; METFORMIN HYDROCHLORIDE

Application Number

21460

Product Number

2

Dosage Form

-

Strength

2.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-21

Regulatory Status

Discontinued

2002
21 Oct
Discontinued Application: 21460

Drug Name

METAGLIP

Product Number

3

Dosage Form

-

Strength

5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-21

21460 / 3

Active Ingredient

GLIPIZIDE; METFORMIN HYDROCHLORIDE

Application Number

21460

Product Number

3

Dosage Form

-

Strength

5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-21

Regulatory Status

Discontinued

1985
14 Feb
Discontinued Application: 88760

Drug Name

MEXATE-AQ

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/ML

Approval Date

1985-02-14

88760 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

88760

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/ML

Approval Date

1985-02-14

Regulatory Status

Discontinued

1989
14 Apr
Discontinued Application: 89887

Drug Name

MEXATE-AQ PRESERVED

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/ML

Approval Date

1989-04-14

89887 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

89887

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/ML

Approval Date

1989-04-14

Regulatory Status

Discontinued

1991
16 May
Discontinued Application: 19915

Drug Name

MONOPRIL

Product Number

2

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-05-16

19915 / 2

Active Ingredient

FOSINOPRIL SODIUM

Application Number

19915

Product Number

2

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-05-16

Regulatory Status

Discontinued

1991
16 May
Discontinued Application: 19915

Drug Name

MONOPRIL

Product Number

3

Dosage Form

-

Strength

20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-05-16

19915 / 3

Active Ingredient

FOSINOPRIL SODIUM

Application Number

19915

Product Number

3

Dosage Form

-

Strength

20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-05-16

Regulatory Status

Discontinued

1995
28 Mar
Discontinued Application: 19915

Drug Name

MONOPRIL

Product Number

4

Dosage Form

-

Strength

40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1995-03-28

19915 / 4

Active Ingredient

FOSINOPRIL SODIUM

Application Number

19915

Product Number

4

Dosage Form

-

Strength

40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1995-03-28

Regulatory Status

Discontinued

1994
30 Nov
Discontinued Application: 20286

Drug Name

MONOPRIL-HCT

Product Number

1

Dosage Form

-

Strength

20MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-11-30

20286 / 1

Active Ingredient

FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

Application Number

20286

Product Number

1

Dosage Form

-

Strength

20MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-11-30

Regulatory Status

Discontinued

1994
30 Nov
Discontinued Application: 20286

Drug Name

MONOPRIL-HCT

Product Number

2

Dosage Form

-

Strength

10MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-11-30

20286 / 2

Active Ingredient

FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

Application Number

20286

Product Number

2

Dosage Form

-

Strength

10MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-11-30

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62336

Drug Name

MUTAMYCIN

Product Number

1

Dosage Form

-

Strength

5MG/VIAL

Approval Date

1982-01-01

62336 / 1

Active Ingredient

MITOMYCIN

Application Number

62336

Product Number

1

Dosage Form

-

Strength

5MG/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62336

Drug Name

MUTAMYCIN

Product Number

2

Dosage Form

-

Strength

20MG/VIAL

Approval Date

1982-01-01

62336 / 2

Active Ingredient

MITOMYCIN

Application Number

62336

Product Number

2

Dosage Form

-

Strength

20MG/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988
10 Mar
Discontinued Application: 62336

Drug Name

MUTAMYCIN

Product Number

3

Dosage Form

-

Strength

40MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-03-10

62336 / 3

Active Ingredient

MITOMYCIN

Application Number

62336

Product Number

3

Dosage Form

-

Strength

40MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-03-10

Regulatory Status

Discontinued

1988
28 Jul
Discontinued Application: 71083

Drug Name

NARCAN

Product Number

1

Dosage Form

-

Strength

0.4MG/ML

Approval Date

1988-07-28

71083 / 1

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

71083

Product Number

1

Dosage Form

-

Strength

0.4MG/ML

Approval Date

1988-07-28

Regulatory Status

Discontinued

1988
28 Jul
Discontinued Application: 71084

Drug Name

NARCAN

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1988-07-28

71084 / 1

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

71084

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1988-07-28

Regulatory Status

Discontinued

1988
28 Jul
Discontinued Application: 71311

Drug Name

NARCAN

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1988-07-28

71311 / 1

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

71311

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1988-07-28

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60365

Drug Name

NEOMYCIN SULFATE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

60365 / 1

Active Ingredient

NEOMYCIN SULFATE

Application Number

60365

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988
16 Feb
Discontinued Application: 72035

Drug Name

NUPRIN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1988-02-16

72035 / 1

Active Ingredient

IBUPROFEN

Application Number

72035

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1988-02-16

Regulatory Status

Discontinued

1988
16 Feb
Discontinued Application: 72036

Drug Name

NUPRIN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1988-02-16

72036 / 1

Active Ingredient

IBUPROFEN

Application Number

72036

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1988-02-16

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 8392

Drug Name

NYDRAZID

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

8392 / 3

Active Ingredient

ISONIAZID

Application Number

8392

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11359

Drug Name

ORA-TESTRYL

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

11359 / 1

Active Ingredient

FLUOXYMESTERONE

Application Number

11359

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11359

Drug Name

ORA-TESTRYL

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

11359 / 2

Active Ingredient

FLUOXYMESTERONE

Application Number

11359

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85910

Drug Name

OXYCODONE 2.5/APAP 500

Product Number

1

Dosage Form

-

Strength

500MG;2.5MG

Approval Date

1982-01-01

85910 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

85910

Product Number

1

Dosage Form

-

Strength

500MG;2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85911

Drug Name

OXYCODONE 5/APAP 500

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1982-01-01

85911 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

85911

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61935

Drug Name

PENICILLIN G SODIUM

Product Number

1

Dosage Form

-

Strength

5,000,000 UNITS/VIAL

Approval Date

1982-01-01

61935 / 1

Active Ingredient

PENICILLIN G SODIUM

Application Number

61935

Product Number

1

Dosage Form

-

Strength

5,000,000 UNITS/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1991
31 Oct
Discontinued Application: 19898

Drug Name

PRAVACHOL

Product Number

2

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-31

19898 / 2

Active Ingredient

PRAVASTATIN SODIUM

Application Number

19898

Product Number

2

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-31

Regulatory Status

Discontinued

1991
31 Oct
Discontinued Application: 19898

Drug Name

PRAVACHOL

Product Number

3

Dosage Form

-

Strength

20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-31

19898 / 3

Active Ingredient

PRAVASTATIN SODIUM

Application Number

19898

Product Number

3

Dosage Form

-

Strength

20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-31

Regulatory Status

Discontinued

1993
22 Mar
Discontinued Application: 19898

Drug Name

PRAVACHOL

Product Number

4

Dosage Form

-

Strength

40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-03-22

19898 / 4

Active Ingredient

PRAVASTATIN SODIUM

Application Number

19898

Product Number

4

Dosage Form

-

Strength

40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-03-22

Regulatory Status

Discontinued

2001
18 Dec
Discontinued Application: 19898

Drug Name

PRAVACHOL

Product Number

8

Dosage Form

-

Strength

80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2001-12-18

19898 / 8

Active Ingredient

PRAVASTATIN SODIUM

Application Number

19898

Product Number

8

Dosage Form

-

Strength

80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2001-12-18

Regulatory Status

Discontinued

2003
24 Jun
Discontinued Application: 21387

Drug Name

PRAVIGARD PAC (COPACKAGED)

Product Number

1

Dosage Form

-

Strength

81MG;20MG

Approval Date

2003-06-24

21387 / 1

Active Ingredient

ASPIRIN; PRAVASTATIN SODIUM

Application Number

21387

Product Number

1

Dosage Form

-

Strength

81MG;20MG

Approval Date

2003-06-24

Regulatory Status

Discontinued

2003
24 Jun
Discontinued Application: 21387

Drug Name

PRAVIGARD PAC (COPACKAGED)

Product Number

2

Dosage Form

-

Strength

81MG;40MG

Approval Date

2003-06-24

21387 / 2

Active Ingredient

ASPIRIN; PRAVASTATIN SODIUM

Application Number

21387

Product Number

2

Dosage Form

-

Strength

81MG;40MG

Approval Date

2003-06-24

Regulatory Status

Discontinued

2003
24 Jun
Discontinued Application: 21387

Drug Name

PRAVIGARD PAC (COPACKAGED)

Product Number

3

Dosage Form

-

Strength

81MG;80MG

Approval Date

2003-06-24

21387 / 3

Active Ingredient

ASPIRIN; PRAVASTATIN SODIUM

Application Number

21387

Product Number

3

Dosage Form

-

Strength

81MG;80MG

Approval Date

2003-06-24

Regulatory Status

Discontinued

2003
24 Jun
Discontinued Application: 21387

Drug Name

PRAVIGARD PAC (COPACKAGED)

Product Number

4

Dosage Form

-

Strength

325MG;20MG

Approval Date

2003-06-24

21387 / 4

Active Ingredient

ASPIRIN; PRAVASTATIN SODIUM

Application Number

21387

Product Number

4

Dosage Form

-

Strength

325MG;20MG

Approval Date

2003-06-24

Regulatory Status

Discontinued

2003
24 Jun
Discontinued Application: 21387

Drug Name

PRAVIGARD PAC (COPACKAGED)

Product Number

5

Dosage Form

-

Strength

325MG;40MG

Approval Date

2003-06-24

21387 / 5

Active Ingredient

ASPIRIN; PRAVASTATIN SODIUM

Application Number

21387

Product Number

5

Dosage Form

-

Strength

325MG;40MG

Approval Date

2003-06-24

Regulatory Status

Discontinued

2003
24 Jun
Discontinued Application: 21387

Drug Name

PRAVIGARD PAC (COPACKAGED)

Product Number

6

Dosage Form

-

Strength

325MG;80MG

Approval Date

2003-06-24

21387 / 6

Active Ingredient

ASPIRIN; PRAVASTATIN SODIUM

Application Number

21387

Product Number

6

Dosage Form

-

Strength

325MG;80MG

Approval Date

2003-06-24

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61392

Drug Name

PRINCIPEN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

61392 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61392

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61392

Drug Name

PRINCIPEN

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

61392 / 2

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61392

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16727

Drug Name

PROLIXIN DECANOATE

Product Number

1

Dosage Form

-

Strength

25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

16727 / 1

Active Ingredient

FLUPHENAZINE DECANOATE

Application Number

16727

Product Number

1

Dosage Form

-

Strength

25MG/ML **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: 16640

Drug Name

QUESTRAN

Product Number

1

Dosage Form

-

Strength

EQ 4GM RESIN/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

16640 / 1

Active Ingredient

CHOLESTYRAMINE

Application Number

16640

Product Number

1

Dosage Form

-

Strength

EQ 4GM RESIN/PACKET **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: 16640

Drug Name

QUESTRAN

Product Number

3

Dosage Form

-

Strength

EQ 4GM RESIN/SCOOPFUL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

16640 / 3

Active Ingredient

CHOLESTYRAMINE

Application Number

16640

Product Number

3

Dosage Form

-

Strength

EQ 4GM RESIN/SCOOPFUL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988
05 Dec
Discontinued Application: 19669

Drug Name

QUESTRAN LIGHT

Product Number

1

Dosage Form

-

Strength

EQ 4GM RESIN/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-12-05

19669 / 1

Active Ingredient

CHOLESTYRAMINE

Application Number

19669

Product Number

1

Dosage Form

-

Strength

EQ 4GM RESIN/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-12-05

Regulatory Status

Discontinued

1988
05 Dec
Discontinued Application: 19669

Drug Name

QUESTRAN LIGHT

Product Number

3

Dosage Form

-

Strength

EQ 4GM RESIN/SCOOPFUL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-12-05

19669 / 3

Active Ingredient

CHOLESTYRAMINE

Application Number

19669

Product Number

3

Dosage Form

-

Strength

EQ 4GM RESIN/SCOOPFUL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-12-05

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9357

Drug Name

RAU-SED

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

9357 / 1

Active Ingredient

RESERPINE

Application Number

9357

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9357

Drug Name

RAU-SED

Product Number

4

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

9357 / 4

Active Ingredient

RESERPINE

Application Number

9357

Product Number

4

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9357

Drug Name

RAU-SED

Product Number

6

Dosage Form

-

Strength

0.5MG

Approval Date

1982-01-01

9357 / 6

Active Ingredient

RESERPINE

Application Number

9357

Product Number

6

Dosage Form

-

Strength

0.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9357

Drug Name

RAU-SED

Product Number

8

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

9357 / 8

Active Ingredient

RESERPINE

Application Number

9357

Product Number

8

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83176

Drug Name

REMSED

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

83176 / 1

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

83176

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83176

Drug Name

REMSED

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

83176 / 2

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

83176

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2003
20 Jun
Discontinued Application: 21567

Drug Name

REYATAZ

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-06-20

21567 / 1

Active Ingredient

ATAZANAVIR SULFATE

Application Number

21567

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-06-20

Regulatory Status

Discontinued

2003
20 Jun
Discontinued Application: 21567

Drug Name

REYATAZ

Product Number

2

Dosage Form

-

Strength

EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-06-20

21567 / 2

Active Ingredient

ATAZANAVIR SULFATE

Application Number

21567

Product Number

2

Dosage Form

-

Strength

EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-06-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9052

Drug Name

REZIPAS

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/GM

Approval Date

1982-01-01

9052 / 1

Active Ingredient

AMINOSALICYLIC ACID RESIN COMPLEX

Application Number

9052

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/GM

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989
13 Apr
Discontinued Application: 62926

Drug Name

RUBEX

Product Number

1

Dosage Form

-

Strength

10MG/VIAL

Approval Date

1989-04-13

62926 / 1

Active Ingredient

DOXORUBICIN HYDROCHLORIDE

Application Number

62926

Product Number

1

Dosage Form

-

Strength

10MG/VIAL

Approval Date

1989-04-13

Regulatory Status

Discontinued

1989
13 Apr
Discontinued Application: 62926

Drug Name

RUBEX

Product Number

2

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1989-04-13

62926 / 2

Active Ingredient

DOXORUBICIN HYDROCHLORIDE

Application Number

62926

Product Number

2

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1989-04-13

Regulatory Status

Discontinued

1989
13 Apr
Discontinued Application: 62926

Drug Name

RUBEX

Product Number

3

Dosage Form

-

Strength

100MG/VIAL

Approval Date

1989-04-13

62926 / 3

Active Ingredient

DOXORUBICIN HYDROCHLORIDE

Application Number

62926

Product Number

3

Dosage Form

-

Strength

100MG/VIAL

Approval Date

1989-04-13

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 6799

Drug Name

RUBRAMIN PC

Product Number

2

Dosage Form

-

Strength

0.1MG/ML

Approval Date

1982-01-01

6799 / 2

Active Ingredient

CYANOCOBALAMIN

Application Number

6799

Product Number

2

Dosage Form

-

Strength

0.1MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 6799

Drug Name

RUBRAMIN PC

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-01-01

6799 / 4

Active Ingredient

CYANOCOBALAMIN

Application Number

6799

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988
28 Apr
Discontinued Application: 6799

Drug Name

RUBRAMIN PC

Product Number

10

Dosage Form

-

Strength

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

Approval Date

1988-04-28

6799 / 10

Active Ingredient

CYANOCOBALAMIN

Application Number

6799

Product Number

10

Dosage Form

-

Strength

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

Approval Date

1988-04-28

Regulatory Status

Discontinued

1994
22 Dec
Discontinued Application: 20152

Drug Name

SERZONE

Product Number

1

Dosage Form

-

Strength

50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-22

20152 / 1

Active Ingredient

NEFAZODONE HYDROCHLORIDE

Application Number

20152

Product Number

1

Dosage Form

-

Strength

50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-22

Regulatory Status

Discontinued

1994
22 Dec
Discontinued Application: 20152

Drug Name

SERZONE

Product Number

2

Dosage Form

-

Strength

100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-22

20152 / 2

Active Ingredient

NEFAZODONE HYDROCHLORIDE

Application Number

20152

Product Number

2

Dosage Form

-

Strength

100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-22

Regulatory Status

Discontinued

1994
22 Dec
Discontinued Application: 20152

Drug Name

SERZONE

Product Number

3

Dosage Form

-

Strength

150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-22

20152 / 3

Active Ingredient

NEFAZODONE HYDROCHLORIDE

Application Number

20152

Product Number

3

Dosage Form

-

Strength

150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-22

Regulatory Status

Discontinued

1994
22 Dec
Discontinued Application: 20152

Drug Name

SERZONE

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1994-12-22

20152 / 4

Active Ingredient

NEFAZODONE HYDROCHLORIDE

Application Number

20152

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1994-12-22

Regulatory Status

Discontinued

1994
22 Dec
Discontinued Application: 20152

Drug Name

SERZONE

Product Number

5

Dosage Form

-

Strength

250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-22

20152 / 5

Active Ingredient

NEFAZODONE HYDROCHLORIDE

Application Number

20152

Product Number

5

Dosage Form

-

Strength

250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-22

Regulatory Status

Discontinued

1994
22 Dec
Discontinued Application: 20152

Drug Name

SERZONE

Product Number

6

Dosage Form

-

Strength

300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-22

20152 / 6

Active Ingredient

NEFAZODONE HYDROCHLORIDE

Application Number

20152

Product Number

6

Dosage Form

-

Strength

300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-22

Regulatory Status

Discontinued

1991
12 Dec
Discontinued Application: 19890

Drug Name

STADOL

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1991-12-12

19890 / 1

Active Ingredient

BUTORPHANOL TARTRATE

Application Number

19890

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1991-12-12

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50526

Drug Name

STATICIN

Product Number

1

Dosage Form

-

Strength

1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50526 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

50526

Product Number

1

Dosage Form

-

Strength

1.5% **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: 4056

Drug Name

STILBESTROL

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

4056 / 1

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBESTROL

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

1982-01-01

4056 / 2

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBESTROL

Product Number

3

Dosage Form

-

Strength

0.2MG/ML

Approval Date

1982-01-01

4056 / 3

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

3

Dosage Form

-

Strength

0.2MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBESTROL

Product Number

4

Dosage Form

-

Strength

0.5MG/ML

Approval Date

1982-01-01

4056 / 4

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

4

Dosage Form

-

Strength

0.5MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBESTROL

Product Number

5

Dosage Form

-

Strength

1MG/ML

Approval Date

1982-01-01

4056 / 5

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

5

Dosage Form

-

Strength

1MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBESTROL

Product Number

6

Dosage Form

-

Strength

5MG/ML

Approval Date

1982-01-01

4056 / 6

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

6

Dosage Form

-

Strength

5MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBETIN

Product Number

7

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

4056 / 7

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

7

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBETIN

Product Number

8

Dosage Form

-

Strength

0.5MG

Approval Date

1982-01-01

4056 / 8

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

8

Dosage Form

-

Strength

0.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBETIN

Product Number

9

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

4056 / 9

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

9

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBETIN

Product Number

10

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

4056 / 10

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

10

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBETIN

Product Number

11

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

4056 / 11

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

11

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBETIN

Product Number

12

Dosage Form

-

Strength

0.5MG

Approval Date

1982-01-01

4056 / 12

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

12

Dosage Form

-

Strength

0.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBETIN

Product Number

13

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

4056 / 13

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

13

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBETIN

Product Number

14

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

4056 / 14

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

14

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 4056

Drug Name

STILBETIN

Product Number

17

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

4056 / 17

Active Ingredient

DIETHYLSTILBESTROL

Application Number

4056

Product Number

17

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1998
17 Sep
Discontinued Application: 20972

Drug Name

SUSTIVA

Product Number

1

Dosage Form

-

Strength

50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-09-17

20972 / 1

Active Ingredient

EFAVIRENZ

Application Number

20972

Product Number

1

Dosage Form

-

Strength

50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-09-17

Regulatory Status

Discontinued

1998
17 Sep
Discontinued Application: 20972

Drug Name

SUSTIVA

Product Number

2

Dosage Form

-

Strength

100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-09-17

20972 / 2

Active Ingredient

EFAVIRENZ

Application Number

20972

Product Number

2

Dosage Form

-

Strength

100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-09-17

Regulatory Status

Discontinued

1998
17 Sep
Discontinued Application: 20972

Drug Name

SUSTIVA

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1998-09-17

20972 / 3

Active Ingredient

EFAVIRENZ

Application Number

20972

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1998-09-17

Regulatory Status

Discontinued

2002
01 Feb
Discontinued Application: 21360

Drug Name

SUSTIVA

Product Number

1

Dosage Form

-

Strength

300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-02-01

21360 / 1

Active Ingredient

EFAVIRENZ

Application Number

21360

Product Number

1

Dosage Form

-

Strength

300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-02-01

Regulatory Status

Discontinued

2002
01 Feb
Discontinued Application: 21360

Drug Name

SUSTIVA

Product Number

2

Dosage Form

-

Strength

600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-02-01

21360 / 2

Active Ingredient

EFAVIRENZ

Application Number

21360

Product Number

2

Dosage Form

-

Strength

600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-02-01

Regulatory Status

Discontinued

1983
09 Mar
Discontinued Application: 62436

Drug Name

T-STAT

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1983-03-09

62436 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

62436

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1983-03-09

Regulatory Status

Discontinued

1987
23 Jul
Discontinued Application: 62748

Drug Name

T-STAT

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1987-07-23

62748 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

62748

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1987-07-23

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11950

Drug Name

TACARYL

Product Number

6

Dosage Form

-

Strength

8MG

Approval Date

1982-01-01

11950 / 6

Active Ingredient

METHDILAZINE HYDROCHLORIDE

Application Number

11950

Product Number

6

Dosage Form

-

Strength

8MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11950

Drug Name

TACARYL

Product Number

7

Dosage Form

-

Strength

4MG/5ML

Approval Date

1982-01-01

11950 / 7

Active Ingredient

METHDILAZINE HYDROCHLORIDE

Application Number

11950

Product Number

7

Dosage Form

-

Strength

4MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11950

Drug Name

TACARYL

Product Number

9

Dosage Form

-

Strength

3.6MG

Approval Date

1982-01-01

11950 / 9

Active Ingredient

METHDILAZINE

Application Number

11950

Product Number

9

Dosage Form

-

Strength

3.6MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 6904

Drug Name

TERFONYL

Product Number

1

Dosage Form

-

Strength

167MG;167MG;167MG

Approval Date

1982-01-01

6904 / 1

Active Ingredient

TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE)

Application Number

6904

Product Number

1

Dosage Form

-

Strength

167MG;167MG;167MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 6904

Drug Name

TERFONYL

Product Number

2

Dosage Form

-

Strength

167MG/5ML;167MG/5ML;167MG/5ML

Approval Date

1982-01-01

6904 / 2

Active Ingredient

TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE)

Application Number

6904

Product Number

2

Dosage Form

-

Strength

167MG/5ML;167MG/5ML;167MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16118

Drug Name

TESLAC

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

16118 / 1

Active Ingredient

TESTOLACTONE

Application Number

16118

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16118

Drug Name

TESLAC

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

16118 / 2

Active Ingredient

TESTOLACTONE

Application Number

16118

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16119

Drug Name

TESLAC

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

16119 / 1

Active Ingredient

TESTOLACTONE

Application Number

16119

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 5657

Drug Name

TUBOCURARINE CHLORIDE

Product Number

1

Dosage Form

-

Strength

3MG/ML

Approval Date

1982-01-01

5657 / 1

Active Ingredient

TUBOCURARINE CHLORIDE

Application Number

5657

Product Number

1

Dosage Form

-

Strength

3MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50530

Drug Name

VELOSEF

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

1982-01-01

50530 / 1

Active Ingredient

CEPHRADINE

Application Number

50530

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11123

Drug Name

VESPRIN

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

11123 / 1

Active Ingredient

TRIFLUPROMAZINE HYDROCHLORIDE

Application Number

11123

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11123

Drug Name

VESPRIN

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

11123 / 2

Active Ingredient

TRIFLUPROMAZINE HYDROCHLORIDE

Application Number

11123

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11123

Drug Name

VESPRIN

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

11123 / 3

Active Ingredient

TRIFLUPROMAZINE HYDROCHLORIDE

Application Number

11123

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1991
09 Oct
Discontinued Application: 20154

Drug Name

VIDEX

Product Number

2

Dosage Form

-

Strength

25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-09

20154 / 2

Active Ingredient

DIDANOSINE

Application Number

20154

Product Number

2

Dosage Form

-

Strength

25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-09

Regulatory Status

Discontinued

1991
09 Oct
Discontinued Application: 20154

Drug Name

VIDEX

Product Number

3

Dosage Form

-

Strength

50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-09

20154 / 3

Active Ingredient

DIDANOSINE

Application Number

20154

Product Number

3

Dosage Form

-

Strength

50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-09

Regulatory Status

Discontinued

1991
09 Oct
Discontinued Application: 20154

Drug Name

VIDEX

Product Number

4

Dosage Form

-

Strength

100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-09

20154 / 4

Active Ingredient

DIDANOSINE

Application Number

20154

Product Number

4

Dosage Form

-

Strength

100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-09

Regulatory Status

Discontinued

1991
09 Oct
Discontinued Application: 20154

Drug Name

VIDEX

Product Number

5

Dosage Form

-

Strength

150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-09

20154 / 5

Active Ingredient

DIDANOSINE

Application Number

20154

Product Number

5

Dosage Form

-

Strength

150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1991-10-09

Regulatory Status

Discontinued

1999
28 Oct
Discontinued Application: 20154

Drug Name

VIDEX

Product Number

6

Dosage Form

-

Strength

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

Approval Date

1999-10-28

20154 / 6

Active Ingredient

DIDANOSINE

Application Number

20154

Product Number

6

Dosage Form

-

Strength

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

Approval Date

1999-10-28

Regulatory Status

Discontinued

1991
09 Oct
Discontinued Application: 20155

Drug Name

VIDEX

Product Number

3

Dosage Form

-

Strength

100MG/PACKET

Approval Date

1991-10-09

20155 / 3

Active Ingredient

DIDANOSINE

Application Number

20155

Product Number

3

Dosage Form

-

Strength

100MG/PACKET

Approval Date

1991-10-09

Regulatory Status

Discontinued

1991
09 Oct
Discontinued Application: 20155

Drug Name

VIDEX

Product Number

4

Dosage Form

-

Strength

167MG/PACKET

Approval Date

1991-10-09

20155 / 4

Active Ingredient

DIDANOSINE

Application Number

20155

Product Number

4

Dosage Form

-

Strength

167MG/PACKET

Approval Date

1991-10-09

Regulatory Status

Discontinued

1991
09 Oct
Discontinued Application: 20155

Drug Name

VIDEX

Product Number

5

Dosage Form

-

Strength

250MG/PACKET

Approval Date

1991-10-09

20155 / 5

Active Ingredient

DIDANOSINE

Application Number

20155

Product Number

5

Dosage Form

-

Strength

250MG/PACKET

Approval Date

1991-10-09

Regulatory Status

Discontinued

1991
09 Oct
Discontinued Application: 20155

Drug Name

VIDEX

Product Number

6

Dosage Form

-

Strength

375MG/PACKET

Approval Date

1991-10-09

20155 / 6

Active Ingredient

DIDANOSINE

Application Number

20155

Product Number

6

Dosage Form

-

Strength

375MG/PACKET

Approval Date

1991-10-09

Regulatory Status

Discontinued

2000
31 Oct
Discontinued Application: 21183

Drug Name

VIDEX EC

Product Number

1

Dosage Form

-

Strength

125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-10-31

21183 / 1

Active Ingredient

DIDANOSINE

Application Number

21183

Product Number

1

Dosage Form

-

Strength

125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-10-31

Regulatory Status

Discontinued

2000
31 Oct
Discontinued Application: 21183

Drug Name

VIDEX EC

Product Number

2

Dosage Form

-

Strength

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

Approval Date

2000-10-31

21183 / 2

Active Ingredient

DIDANOSINE

Application Number

21183

Product Number

2

Dosage Form

-

Strength

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

Approval Date

2000-10-31

Regulatory Status

Discontinued

2000
31 Oct
Discontinued Application: 21183

Drug Name

VIDEX EC

Product Number

3

Dosage Form

-

Strength

250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-10-31

21183 / 3

Active Ingredient

DIDANOSINE

Application Number

21183

Product Number

3

Dosage Form

-

Strength

250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-10-31

Regulatory Status

Discontinued

2000
31 Oct
Discontinued Application: 21183

Drug Name

VIDEX EC

Product Number

4

Dosage Form

-

Strength

400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-10-31

21183 / 4

Active Ingredient

DIDANOSINE

Application Number

21183

Product Number

4

Dosage Form

-

Strength

400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-10-31

Regulatory Status

Discontinued

1988
12 Jul
Discontinued Application: 70867

Drug Name

VINCREX

Product Number

1

Dosage Form

-

Strength

5MG/VIAL

Approval Date

1988-07-12

70867 / 1

Active Ingredient

VINCRISTINE SULFATE

Application Number

70867

Product Number

1

Dosage Form

-

Strength

5MG/VIAL

Approval Date

1988-07-12

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80860

Drug Name

VITAMIN A

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

80860 / 1

Active Ingredient

VITAMIN A PALMITATE

Application Number

80860

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

2002
31 Dec
Discontinued Application: 21453

Drug Name

ZERIT XR

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

2002-12-31

21453 / 1

Active Ingredient

STAVUDINE

Application Number

21453

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

2002-12-31

Regulatory Status

Discontinued

2002
31 Dec
Discontinued Application: 21453

Drug Name

ZERIT XR

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2002-12-31

21453 / 2

Active Ingredient

STAVUDINE

Application Number

21453

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2002-12-31

Regulatory Status

Discontinued

2002
31 Dec
Discontinued Application: 21453

Drug Name

ZERIT XR

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

2002-12-31

21453 / 3

Active Ingredient

STAVUDINE

Application Number

21453

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

2002-12-31

Regulatory Status

Discontinued

2002
31 Dec
Discontinued Application: 21453

Drug Name

ZERIT XR

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2002-12-31

21453 / 4

Active Ingredient

STAVUDINE

Application Number

21453

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2002-12-31

Regulatory Status

Discontinued

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Drug Status Breakdown
182 total
  • Discontinued
Official Source

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

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

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

Drug Name

AMITID

Application Number

86454

Product Number

1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Dosage Form

-

Strength

10MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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