Warner Chilcott Company, LLC Discontinued
FDA Approved Drugs

Warner Chilcott Company, LLC 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 93
  • Latest Approval Date Aug 12, 2005
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
94
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Unclassified
1
View
Discontinued
93
View
Company Overview

Company

Warner Chilcott Company, LLC Discontinued

Country

U.S.A

Website

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Company Snapshot

Warner Chilcott Company, LLC Discontinued

Administrative Headquarters Morris Corporate Center III 400 Interpace Parkway Parsippany

U.S.A

www.wcrx.com/ View on Map
FDA Approved Drug Records ( 93 records )
1982
01 Jan
Discontinued Application: 85218

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

2

Dosage Form

-

Strength

300MG;30MG

Approval Date

1982-01-01

85218 / 2

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

85218

Product Number

2

Dosage Form

-

Strength

300MG;30MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85992

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;15MG

Approval Date

1982-01-01

85992 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

85992

Product Number

1

Dosage Form

-

Strength

300MG;15MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87306

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;60MG

Approval Date

1982-01-01

87306 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

87306

Product Number

1

Dosage Form

-

Strength

300MG;60MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2005
12 Aug
Discontinued Application: 21823

Drug Name

ACTONEL WITH CALCIUM (COPACKAGED)

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE;35MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-08-12

21823 / 1

Active Ingredient

CALCIUM CARBONATE; RISEDRONATE SODIUM

Application Number

21823

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE;35MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-08-12

Regulatory Status

Discontinued

1990
09 Jan
Discontinued Application: 72817

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1990-01-09

72817 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

72817

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1990-01-09

Regulatory Status

Discontinued

1990
09 Jan
Discontinued Application: 72818

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

1990-01-09

72818 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

72818

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

1990-01-09

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83937

Drug Name

AMITRIL

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

83937 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

83937

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83938

Drug Name

AMITRIL

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

83938 / 2

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

83938

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83939

Drug Name

AMITRIL

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

83939 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

83939

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84957

Drug Name

AMITRIL

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1982-01-01

84957 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

84957

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85093

Drug Name

AMITRIL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

85093 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

85093

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86295

Drug Name

AMITRIL

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

1982-01-01

86295 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

86295

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987
02 Jan
Discontinued Application: 70429

Drug Name

CARBAMAZEPINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-01-02

70429 / 1

Active Ingredient

CARBAMAZEPINE

Application Number

70429

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-01-02

Regulatory Status

Discontinued

1983
24 Jan
Discontinued Application: 87515

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-01-24

87515 / 1

Active Ingredient

CHLORTHALIDONE

Application Number

87515

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-01-24

Regulatory Status

Discontinued

1983
09 Feb
Discontinued Application: 87516

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-02-09

87516 / 1

Active Ingredient

CHLORTHALIDONE

Application Number

87516

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-02-09

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86742

Drug Name

CHOLEDYL SA

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1982-01-01

86742 / 1

Active Ingredient

OXTRIPHYLLINE

Application Number

86742

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983
24 May
Discontinued Application: 87863

Drug Name

CHOLEDYL SA

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1983-05-24

87863 / 1

Active Ingredient

OXTRIPHYLLINE

Application Number

87863

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1983-05-24

Regulatory Status

Discontinued

1988
13 Jun
Discontinued Application: 72138

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1988-06-13

72138 / 1

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

72138

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1988-06-13

Regulatory Status

Discontinued

1988
13 Jun
Discontinued Application: 72139

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.2MG

Approval Date

1988-06-13

72139 / 1

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

72139

Product Number

1

Dosage Form

-

Strength

0.2MG

Approval Date

1988-06-13

Regulatory Status

Discontinued

1988
13 Jun
Discontinued Application: 72140

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

1988-06-13

72140 / 1

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

72140

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

1988-06-13

Regulatory Status

Discontinued

1988
01 Mar
Discontinued Application: 71774

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1988-03-01

71774 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71774

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1988-03-01

Regulatory Status

Discontinued

1988
01 Mar
Discontinued Application: 71775

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1988-03-01

71775 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71775

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1988-03-01

Regulatory Status

Discontinued

1988
01 Mar
Discontinued Application: 71776

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1988-03-01

71776 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71776

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1988-03-01

Regulatory Status

Discontinued

1988
03 Mar
Discontinued Application: 71828

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1988-03-03

71828 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71828

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1988-03-03

Regulatory Status

Discontinued

1988
03 Mar
Discontinued Application: 71829

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1988-03-03

71829 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71829

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1988-03-03

Regulatory Status

Discontinued

1988
03 Mar
Discontinued Application: 71830

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1988-03-03

71830 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71830

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1988-03-03

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 7085

Drug Name

CYANOCOBALAMIN

Product Number

2

Dosage Form

-

Strength

1MG/ML

Approval Date

1982-01-01

7085 / 2

Active Ingredient

CYANOCOBALAMIN

Application Number

7085

Product Number

2

Dosage Form

-

Strength

1MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61725

Drug Name

CYCLOPAR

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

61725 / 1

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

61725

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61725

Drug Name

CYCLOPAR

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

61725 / 2

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

61725

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62175

Drug Name

CYCLOPAR

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

62175 / 1

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

62175

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62332

Drug Name

CYCLOPAR

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

62332 / 1

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

62332

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62332

Drug Name

CYCLOPAR

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

62332 / 2

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

62332

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
04 Sep
Discontinued Application: 70209

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1985-09-04

70209 / 1

Active Ingredient

DIAZEPAM

Application Number

70209

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1985-09-04

Regulatory Status

Discontinued

1985
04 Sep
Discontinued Application: 70210

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1985-09-04

70210 / 1

Active Ingredient

DIAZEPAM

Application Number

70210

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1985-09-04

Regulatory Status

Discontinued

1985
04 Sep
Discontinued Application: 70222

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1985-09-04

70222 / 1

Active Ingredient

DIAZEPAM

Application Number

70222

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1985-09-04

Regulatory Status

Discontinued

1987
22 Oct
Discontinued Application: 71613

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1987-10-22

71613 / 1

Active Ingredient

DIAZEPAM

Application Number

71613

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1987-10-22

Regulatory Status

Discontinued

1987
22 Oct
Discontinued Application: 71614

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1987-10-22

71614 / 1

Active Ingredient

DIAZEPAM

Application Number

71614

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1987-10-22

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18138

Drug Name

DOPAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1982-01-01

18138 / 1

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

18138

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
20 Sep
Discontinued Application: 70558

Drug Name

DOPAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1985-09-20

70558 / 1

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

70558

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1985-09-20

Regulatory Status

Discontinued

1985
20 Sep
Discontinued Application: 70559

Drug Name

DOPAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG/ML

Approval Date

1985-09-20

70559 / 1

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

70559

Product Number

1

Dosage Form

-

Strength

80MG/ML

Approval Date

1985-09-20

Regulatory Status

Discontinued

1985
30 Oct
Discontinued Application: 62653

Drug Name

DORYX

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1985-10-30

62653 / 1

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62653

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1985-10-30

Regulatory Status

Discontinued

1985
28 Aug
Discontinued Application: 62593

Drug Name

DOXYCYCLINE HYCLATE

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1985-08-28

62593 / 1

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62593

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1985-08-28

Regulatory Status

Discontinued

1985
05 Dec
Discontinued Application: 62594

Drug Name

DOXYCYCLINE HYCLATE

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1985-12-05

62594 / 1

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62594

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1985-12-05

Regulatory Status

Discontinued

1985
05 Dec
Discontinued Application: 62594

Drug Name

DOXYCYCLINE HYCLATE

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1985-12-05

62594 / 2

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62594

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1985-12-05

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17917

Drug Name

DURAQUIN

Product Number

1

Dosage Form

-

Strength

330MG

Approval Date

1982-01-01

17917 / 1

Active Ingredient

QUINIDINE GLUCONATE

Application Number

17917

Product Number

1

Dosage Form

-

Strength

330MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50512

Drug Name

DURICEF

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

50512 / 1

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

50512

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE **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: 50512

Drug Name

DURICEF

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

50512 / 2

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

50512

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50527

Drug Name

DURICEF

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50527 / 1

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

50527

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/5ML **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: 50527

Drug Name

DURICEF

Product Number

2

Dosage Form

-

Strength

EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50527 / 2

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

50527

Product Number

2

Dosage Form

-

Strength

EQ 125MG BASE/5ML **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: 50527

Drug Name

DURICEF

Product Number

3

Dosage Form

-

Strength

EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50527 / 3

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

50527

Product Number

3

Dosage Form

-

Strength

EQ 250MG BASE/5ML **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: 50528

Drug Name

DURICEF

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

50528 / 1

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

50528

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE **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: 62338

Drug Name

ERYC

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

62338 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

62338

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62322

Drug Name

ERYPAR

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

62322 / 1

Active Ingredient

ERYTHROMYCIN STEARATE

Application Number

62322

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1991
30 Apr
Discontinued Application: 72472

Drug Name

FENOPROFEN CALCIUM

Product Number

1

Dosage Form

-

Strength

EQ 300MG BASE

Approval Date

1991-04-30

72472 / 1

Active Ingredient

FENOPROFEN CALCIUM

Application Number

72472

Product Number

1

Dosage Form

-

Strength

EQ 300MG BASE

Approval Date

1991-04-30

Regulatory Status

Discontinued

1991
30 Apr
Discontinued Application: 72946

Drug Name

FENOPROFEN CALCIUM

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE

Approval Date

1991-04-30

72946 / 1

Active Ingredient

FENOPROFEN CALCIUM

Application Number

72946

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE

Approval Date

1991-04-30

Regulatory Status

Discontinued

1987
04 Dec
Discontinued Application: 71767

Drug Name

FLURAZEPAM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1987-12-04

71767 / 1

Active Ingredient

FLURAZEPAM HYDROCHLORIDE

Application Number

71767

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1987-12-04

Regulatory Status

Discontinued

1987
04 Dec
Discontinued Application: 71768

Drug Name

FLURAZEPAM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1987-12-04

71768 / 1

Active Ingredient

FLURAZEPAM HYDROCHLORIDE

Application Number

71768

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1987-12-04

Regulatory Status

Discontinued

1983
31 Jan
Discontinued Application: 18419

Drug Name

FUROSEMIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1983-01-31

18419 / 1

Active Ingredient

FUROSEMIDE

Application Number

18419

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1983-01-31

Regulatory Status

Discontinued

1983
31 Jan
Discontinued Application: 18419

Drug Name

FUROSEMIDE

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

1983-01-31

18419 / 2

Active Ingredient

FUROSEMIDE

Application Number

18419

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

1983-01-31

Regulatory Status

Discontinued

1984
13 Nov
Discontinued Application: 18419

Drug Name

FUROSEMIDE

Product Number

3

Dosage Form

-

Strength

80MG

Approval Date

1984-11-13

18419 / 3

Active Ingredient

FUROSEMIDE

Application Number

18419

Product Number

3

Dosage Form

-

Strength

80MG

Approval Date

1984-11-13

Regulatory Status

Discontinued

1982
26 Feb
Discontinued Application: 18420

Drug Name

FUROSEMIDE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1982-02-26

18420 / 1

Active Ingredient

FUROSEMIDE

Application Number

18420

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1982-02-26

Regulatory Status

Discontinued

1986
10 Mar
Discontinued Application: 19412

Drug Name

HEAD & SHOULDERS CONDITIONER

Product Number

2

Dosage Form

-

Strength

0.3%

Approval Date

1986-03-10

19412 / 2

Active Ingredient

PYRITHIONE ZINC

Application Number

19412

Product Number

2

Dosage Form

-

Strength

0.3%

Approval Date

1986-03-10

Regulatory Status

Discontinued

1982
03 May
Discontinued Application: 87586

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-05-03

87586 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

87586

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-05-03

Regulatory Status

Discontinued

1982
03 May
Discontinued Application: 87587

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-05-03

87587 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

87587

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-05-03

Regulatory Status

Discontinued

1989
11 Oct
Discontinued Application: 63092

Drug Name

KANAMYCIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1989-10-11

63092 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

63092

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1989-10-11

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87225

Drug Name

LABID

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

87225 / 1

Active Ingredient

THEOPHYLLINE

Application Number

87225

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988
12 Jan
Discontinued Application: 71038

Drug Name

LORAZEPAM

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1988-01-12

71038 / 1

Active Ingredient

LORAZEPAM

Application Number

71038

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1988-01-12

Regulatory Status

Discontinued

1988
12 Jan
Discontinued Application: 71039

Drug Name

LORAZEPAM

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1988-01-12

71039 / 1

Active Ingredient

LORAZEPAM

Application Number

71039

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1988-01-12

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50478

Drug Name

NYSERT

Product Number

1

Dosage Form

-

Strength

100,000 UNITS

Approval Date

1982-01-01

50478 / 1

Active Ingredient

NYSTATIN

Application Number

50478

Product Number

1

Dosage Form

-

Strength

100,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86845

Drug Name

ORLEX

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

86845 / 1

Active Ingredient

ACETIC ACID, GLACIAL

Application Number

86845

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86844

Drug Name

ORLEX HC

Product Number

1

Dosage Form

-

Strength

2%;1%

Approval Date

1982-01-01

86844 / 1

Active Ingredient

ACETIC ACID, GLACIAL; HYDROCORTISONE

Application Number

86844

Product Number

1

Dosage Form

-

Strength

2%;1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17716

Drug Name

OVCON-35

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

17716 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

17716

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG **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: 18127

Drug Name

OVCON-35

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

18127 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

18127

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG **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: 17576

Drug Name

OVCON-50

Product Number

1

Dosage Form

-

Strength

0.05MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

17576 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

17576

Product Number

1

Dosage Form

-

Strength

0.05MG;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: 18128

Drug Name

OVCON-50

Product Number

1

Dosage Form

-

Strength

0.05MG;1MG

Approval Date

1982-01-01

18128 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

18128

Product Number

1

Dosage Form

-

Strength

0.05MG;1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1990
30 Mar
Discontinued Application: 89900

Drug Name

PHENYTOIN SODIUM

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1990-03-30

89900 / 1

Active Ingredient

PHENYTOIN SODIUM

Application Number

89900

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1990-03-30

Regulatory Status

Discontinued

1988
03 May
Discontinued Application: 89528

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1988-05-03

89528 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

89528

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1988-05-03

Regulatory Status

Discontinued

1988
03 May
Discontinued Application: 89529

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG/ML

Approval Date

1988-05-03

89529 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

89529

Product Number

1

Dosage Form

-

Strength

500MG/ML

Approval Date

1988-05-03

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83786

Drug Name

PROPOXYPHENE HYDROCHLORIDE 65

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1982-01-01

83786 / 1

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

83786

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
15 Sep
Discontinued Application: 70438

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1986-09-15

70438 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70438

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1986-09-15

Regulatory Status

Discontinued

1986
15 Sep
Discontinued Application: 70439

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1986-09-15

70439 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70439

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1986-09-15

Regulatory Status

Discontinued

1986
15 Sep
Discontinued Application: 70440

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1986-09-15

70440 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70440

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1986-09-15

Regulatory Status

Discontinued

1986
24 Sep
Discontinued Application: 70441

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

1986-09-24

70441 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70441

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

1986-09-24

Regulatory Status

Discontinued

1986
15 Sep
Discontinued Application: 70442

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

1986-09-15

70442 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70442

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

1986-09-15

Regulatory Status

Discontinued

1988
26 Jan
Discontinued Application: 71771

Drug Name

PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;40MG

Approval Date

1988-01-26

71771 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE

Application Number

71771

Product Number

1

Dosage Form

-

Strength

25MG;40MG

Approval Date

1988-01-26

Regulatory Status

Discontinued

1988
26 Jan
Discontinued Application: 71772

Drug Name

PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;80MG

Approval Date

1988-01-26

71772 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE

Application Number

71772

Product Number

1

Dosage Form

-

Strength

25MG;80MG

Approval Date

1988-01-26

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83879

Drug Name

QUINIDINE SULFATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

83879 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

83879

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
18 Nov
Discontinued Application: 87952

Drug Name

SPIRONOLACTONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-11-18

87952 / 1

Active Ingredient

SPIRONOLACTONE

Application Number

87952

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-11-18

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62300

Drug Name

TETRACYCLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

62300 / 1

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

62300

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62300

Drug Name

TETRACYCLINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

62300 / 2

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

62300

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
24 Sep
Discontinued Application: 70340

Drug Name

VERAPAMIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

1986-09-24

70340 / 1

Active Ingredient

VERAPAMIL HYDROCHLORIDE

Application Number

70340

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

1986-09-24

Regulatory Status

Discontinued

1986
24 Sep
Discontinued Application: 70341

Drug Name

VERAPAMIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

120MG

Approval Date

1986-09-24

70341 / 1

Active Ingredient

VERAPAMIL HYDROCHLORIDE

Application Number

70341

Product Number

1

Dosage Form

-

Strength

120MG

Approval Date

1986-09-24

Regulatory Status

Discontinued

1987
14 Jan
Discontinued Application: 70524

Drug Name

VICKS FORMULA 44

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1987-01-14

70524 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

70524

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1987-01-14

Regulatory Status

Discontinued

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Drug Status Breakdown
93 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

ACETAMINOPHEN AND CODEINE PHOSPHATE

Application Number

85218

Product Number

2

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Dosage Form

-

Strength

300MG;30MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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