Forest Laboratories, Inc.
FDA Approved Drugs

Forest Laboratories, Inc.

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 Unclassified

Total Records 61
Latest Approval Date Nov 26, 2004
Data Source FDA
First Approval Date Jan 01, 1982

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Company

Forest Laboratories, Inc.

Country

U.S.A

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Forest Laboratories, Inc.

909 Third Avenue New York, NY 10022

U.S.A

www.allergan.com/ View on Map

FDA Approved Drug Records ( 61 records )

1984

10 Jan

Discontinued Application: 9319

Drug Name

AMBENYL

Product Number

Dosage Form

Strength

12.5MG/5ML;10MG/5ML

Approval Date

1984-01-10

9319 / 6 View Details

Active Ingredient

BROMODIPHENHYDRAMINE HYDROCHLORIDE; CODEINE PHOSPHATE

Application Number

9319

Product Number

Dosage Form

Strength

12.5MG/5ML;10MG/5ML

Approval Date

1984-01-10

Regulatory Status

Discontinued

1986

16 Jan

Discontinued Application: 88889

Drug Name

BANCAP

Product Number

Dosage Form

Strength

325MG;50MG

Approval Date

1986-01-16

88889 / 1 View Details

Active Ingredient

ACETAMINOPHEN; BUTALBITAL

Application Number

88889

Product Number

Dosage Form

Strength

325MG;50MG

Approval Date

1986-01-16

Regulatory Status

Discontinued

1983

17 Mar

Discontinued Application: 87961

Drug Name

BANCAP HC

Product Number

Dosage Form

Strength

500MG;5MG

Approval Date

1983-03-17

87961 / 1 View Details

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

87961

Product Number

Dosage Form

Strength

500MG;5MG

Approval Date

1983-03-17

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 11657

Drug Name

BETAPRONE

Product Number

Dosage Form

Strength

N/A

Approval Date

1982-01-01

11657 / 1 View Details

Active Ingredient

PROPIOLACTONE

Application Number

11657

Product Number

Dosage Form

Strength

N/A

Approval Date

1982-01-01

Regulatory Status

Discontinued

2004

29 Jul

Discontinued Application: 21431

Drug Name

CAMPRAL

Product Number

Dosage Form

Strength

333MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-07-29

21431 / 1 View Details

Active Ingredient

ACAMPROSATE CALCIUM

Application Number

21431

Product Number

Dosage Form

Strength

333MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-07-29

Regulatory Status

Discontinued

1986

14 Aug

Discontinued Application: 70231

Drug Name

CARBAMAZEPINE

Product Number

Dosage Form

Strength

200MG

Approval Date

1986-08-14

70231 / 1 View Details

Active Ingredient

CARBAMAZEPINE

Application Number

70231

Product Number

Dosage Form

Strength

200MG

Approval Date

1986-08-14

Regulatory Status

Discontinued

1999

22 Dec

Discontinued Application: 21046

Drug Name

CELEXA

Product Number

Dosage Form

Strength

EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-12-22

21046 / 1 View Details

Active Ingredient

CITALOPRAM HYDROBROMIDE

Application Number

21046

Product Number

Dosage Form

Strength

EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-12-22

Regulatory Status

Discontinued

2004

26 Nov

Discontinued Application: 21378

Drug Name

COMBUNOX

Product Number

Dosage Form

Strength

400MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-11-26

21378 / 1 View Details

Active Ingredient

IBUPROFEN; OXYCODONE HYDROCHLORIDE

Application Number

21378

Product Number

Dosage Form

Strength

400MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-11-26

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80731

Drug Name

CORTISONE ACETATE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

80731 / 1 View Details

Active Ingredient

CORTISONE ACETATE

Application Number

80731

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85509

Drug Name

DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Product Number

Dosage Form

Strength

0.025MG;2.5MG

Approval Date

1982-01-01

85509 / 1 View Details

Active Ingredient

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Application Number

85509

Product Number

Dosage Form

Strength

0.025MG;2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983

17 Mar

Discontinued Application: 87809

Drug Name

DURADYNE DHC

Product Number

Dosage Form

Strength

500MG;5MG

Approval Date

1983-03-17

87809 / 1 View Details

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

87809

Product Number

Dosage Form

Strength

500MG;5MG

Approval Date

1983-03-17

Regulatory Status

Discontinued

1985

03 Apr

Discontinued Application: 88503

Drug Name

DURAPHYL

Product Number

Dosage Form

Strength

100MG

Approval Date

1985-04-03

88503 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

88503

Product Number

Dosage Form

Strength

100MG

Approval Date

1985-04-03

Regulatory Status

Discontinued

1985

03 Apr

Discontinued Application: 88504

Drug Name

DURAPHYL

Product Number

Dosage Form

Strength

200MG

Approval Date

1985-04-03

88504 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

88504

Product Number

Dosage Form

Strength

200MG

Approval Date

1985-04-03

Regulatory Status

Discontinued

1985

03 Apr

Discontinued Application: 88505

Drug Name

DURAPHYL

Product Number

Dosage Form

Strength

300MG

Approval Date

1985-04-03

88505 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

88505

Product Number

Dosage Form

Strength

300MG

Approval Date

1985-04-03

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85502

Drug Name

ELIXICON

Product Number

Dosage Form

Strength

100MG/5ML

Approval Date

1982-01-01

85502 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

85502

Product Number

Dosage Form

Strength

100MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984

31 Jul

Discontinued Application: 83921

Drug Name

ELIXOPHYLLIN

Product Number

Dosage Form

Strength

200MG

Approval Date

1984-07-31

83921 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

83921

Product Number

Dosage Form

Strength

200MG

Approval Date

1984-07-31

Regulatory Status

Discontinued

1984

31 Jul

Discontinued Application: 85545

Drug Name

ELIXOPHYLLIN

Product Number

Dosage Form

Strength

100MG

Approval Date

1984-07-31

85545 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

85545

Product Number

Dosage Form

Strength

100MG

Approval Date

1984-07-31

Regulatory Status

Discontinued

1985

29 Jan

Discontinued Application: 86826

Drug Name

ELIXOPHYLLIN SR

Product Number

Dosage Form

Strength

125MG

Approval Date

1985-01-29

86826 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

86826

Product Number

Dosage Form

Strength

125MG

Approval Date

1985-01-29

Regulatory Status

Discontinued

1985

29 Jan

Discontinued Application: 86826

Drug Name

ELIXOPHYLLIN SR

Product Number

Dosage Form

Strength

250MG

Approval Date

1985-01-29

86826 / 2 View Details

Active Ingredient

THEOPHYLLINE

Application Number

86826

Product Number

Dosage Form

Strength

250MG

Approval Date

1985-01-29

Regulatory Status

Discontinued

1988

23 Dec

Discontinued Application: 89660

Drug Name

ESGIC

Product Number

Dosage Form

Strength

325MG;50MG;40MG

Approval Date

1988-12-23

89660 / 1 View Details

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

89660

Product Number

Dosage Form

Strength

325MG;50MG;40MG

Approval Date

1988-12-23

Regulatory Status

Discontinued

1993

17 Sep

Discontinued Application: 19650

Drug Name

FLUMADINE

Product Number

Dosage Form

Strength

50MG/5ML

Approval Date

1993-09-17

19650 / 1 View Details

Active Ingredient

RIMANTADINE HYDROCHLORIDE

Application Number

19650

Product Number

Dosage Form

Strength

50MG/5ML

Approval Date

1993-09-17

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85136

Drug Name

FORBAXIN

Product Number

Dosage Form

Strength

750MG

Approval Date

1982-01-01

85136 / 1 View Details

Active Ingredient

METHOCARBAMOL

Application Number

85136

Product Number

Dosage Form

Strength

750MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84776

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

84776 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

84776

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84776

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

84776 / 2 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

84776

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85067

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

85067 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

85067

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80732

Drug Name

HYDROCORTISONE

Product Number

Dosage Form

Strength

20MG

Approval Date

1982-01-01

80732 / 1 View Details

Active Ingredient

HYDROCORTISONE

Application Number

80732

Product Number

Dosage Form

Strength

20MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989

15 Mar

Discontinued Application: 72410

Drug Name

INDOMETHACIN

Product Number

Dosage Form

Strength

75MG

Approval Date

1989-03-15

72410 / 1 View Details

Active Ingredient

INDOMETHACIN

Application Number

72410

Product Number

Dosage Form

Strength

75MG

Approval Date

1989-03-15

Regulatory Status

Discontinued

Unclassified Application: 21440

Drug Name

LEXAPRO

Product Number

Dosage Form

Strength

EQ 5MG BASE

Approval Date

21440 / 1 View Details

Active Ingredient

ESCITALOPRAM OXALATE

Application Number

21440

Product Number

Dosage Form

Strength

EQ 5MG BASE

Approval Date

Regulatory Status

Unclassified

Unclassified Application: 21440

Drug Name

LEXAPRO

Product Number

Dosage Form

Strength

EQ 10MG BASE

Approval Date

21440 / 2 View Details

Active Ingredient

ESCITALOPRAM OXALATE

Application Number

21440

Product Number

Dosage Form

Strength

EQ 10MG BASE

Approval Date

Regulatory Status

Unclassified

Unclassified Application: 21440

Drug Name

LEXAPRO

Product Number

Dosage Form

Strength

EQ 20MG BASE

Approval Date

21440 / 3 View Details

Active Ingredient

ESCITALOPRAM OXALATE

Application Number

21440

Product Number

Dosage Form

Strength

EQ 20MG BASE

Approval Date

Regulatory Status

Unclassified

1982

01 Jan

Discontinued Application: 85137

Drug Name

METHOCARBAMOL

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

85137 / 1 View Details

Active Ingredient

METHOCARBAMOL

Application Number

85137

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80839

Drug Name

METHYLTESTOSTERONE

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

80839 / 1 View Details

Active Ingredient

METHYLTESTOSTERONE

Application Number

80839

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80973

Drug Name

METHYLTESTOSTERONE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

80973 / 1 View Details

Active Ingredient

METHYLTESTOSTERONE

Application Number

80973

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83754

Drug Name

METRA

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

83754 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

83754

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86012

Drug Name

MICROSUL

Product Number

Dosage Form

Strength

1GM

Approval Date

1982-01-01

86012 / 1 View Details

Active Ingredient

SULFAMETHIZOLE

Application Number

86012

Product Number

Dosage Form

Strength

1GM

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84740

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

84740 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

84740

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84741

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

84741 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

84741

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84742

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

84742 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

84742

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84743

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

84743 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

84743

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80748

Drug Name

PREDNISOLONE

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

80748 / 1 View Details

Active Ingredient

PREDNISOLONE

Application Number

80748

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80279

Drug Name

PREDNISONE

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

80279 / 1 View Details

Active Ingredient

PREDNISONE

Application Number

80279

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80306

Drug Name

PREDNISONE

Product Number

Dosage Form

Strength

2.5MG

Approval Date

1982-01-01

80306 / 1 View Details

Active Ingredient

PREDNISONE

Application Number

80306

Product Number

Dosage Form

Strength

2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80328

Drug Name

PREDNISONE

Product Number

Dosage Form

Strength

1MG

Approval Date

1982-01-01

80328 / 1 View Details

Active Ingredient

PREDNISONE

Application Number

80328

Product Number

Dosage Form

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989

06 Mar

Discontinued Application: 89840

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

Dosage Form

Strength

500MG

Approval Date

1989-03-06

89840 / 1 View Details

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

89840

Product Number

Dosage Form

Strength

500MG

Approval Date

1989-03-06

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80273

Drug Name

PROKLAR

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

80273 / 1 View Details

Active Ingredient

SULFAMETHIZOLE

Application Number

80273

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989

11 Apr

Discontinued Application: 72499

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

Dosage Form

Strength

60MG

Approval Date

1989-04-11

72499 / 1 View Details

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

72499

Product Number

Dosage Form

Strength

60MG

Approval Date

1989-04-11

Regulatory Status

Discontinued

1989

11 Apr

Discontinued Application: 72500

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

Dosage Form

Strength

80MG

Approval Date

1989-04-11

72500 / 1 View Details

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

72500

Product Number

Dosage Form

Strength

80MG

Approval Date

1989-04-11

Regulatory Status

Discontinued

1989

11 Apr

Discontinued Application: 72501

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

Dosage Form

Strength

120MG

Approval Date

1989-04-11

72501 / 1 View Details

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

72501

Product Number

Dosage Form

Strength

120MG

Approval Date

1989-04-11

Regulatory Status

Discontinued

1989

11 Apr

Discontinued Application: 72502

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

Dosage Form

Strength

160MG

Approval Date

1989-04-11

72502 / 1 View Details

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

72502

Product Number

Dosage Form

Strength

160MG

Approval Date

1989-04-11

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 61606

Drug Name

PYOCIDIN

Product Number

Dosage Form

Strength

5MG/ML;EQ 10,000 UNITS BASE/ML

Approval Date

1982-01-01

61606 / 1 View Details

Active Ingredient

HYDROCORTISONE; POLYMYXIN B SULFATE

Application Number

61606

Product Number

Dosage Form

Strength

5MG/ML;EQ 10,000 UNITS BASE/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80099

Drug Name

SULFALOID

Product Number

Dosage Form

Strength

167MG;167MG;167MG

Approval Date

1982-01-01

80099 / 1 View Details

Active Ingredient

TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE)

Application Number

80099

Product Number

Dosage Form

Strength

167MG;167MG;167MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80100

Drug Name

SULFALOID

Product Number

Dosage Form

Strength

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

Approval Date

1982-01-01

80100 / 1 View Details

Active Ingredient

TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE)

Application Number

80100

Product Number

Dosage Form

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 7942

Drug Name

SUS-PHRINE SULFITE FREE

Product Number

Dosage Form

Strength

5MG/ML

Approval Date

1982-01-01

7942 / 1 View Details

Active Ingredient

EPINEPHRINE

Application Number

7942

Product Number

Dosage Form

Strength

5MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1999

05 Feb

Discontinued Application: 7942

Drug Name

SUS-PHRINE SULFITE FREE

Product Number

Dosage Form

Strength

1.5MG/AMP

Approval Date

1999-02-05

7942 / 3 View Details

Active Ingredient

EPINEPHRINE

Application Number

7942

Product Number

Dosage Form

Strength

1.5MG/AMP

Approval Date

1999-02-05

Regulatory Status

Discontinued

1995

28 Apr

Discontinued Application: 40034

Drug Name

THEOPHYLLINE

Product Number

Dosage Form

Strength

450MG

Approval Date

1995-04-28

40034 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

40034

Product Number

Dosage Form

Strength

450MG

Approval Date

1995-04-28

Regulatory Status

Discontinued

1994

14 Feb

Discontinued Application: 40052

Drug Name

THEOPHYLLINE

Product Number

Dosage Form

Strength

100MG

Approval Date

1994-02-14

40052 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

40052

Product Number

Dosage Form

Strength

100MG

Approval Date

1994-02-14

Regulatory Status

Discontinued

1994

14 Feb

Discontinued Application: 40052

Drug Name

THEOPHYLLINE

Product Number

Dosage Form

Strength

125MG

Approval Date

1994-02-14

40052 / 2 View Details

Active Ingredient

THEOPHYLLINE

Application Number

40052

Product Number

Dosage Form

Strength

125MG

Approval Date

1994-02-14

Regulatory Status

Discontinued

1994

14 Feb

Discontinued Application: 40052

Drug Name

THEOPHYLLINE

Product Number

Dosage Form

Strength

200MG

Approval Date

1994-02-14

40052 / 3 View Details

Active Ingredient

THEOPHYLLINE

Application Number

40052

Product Number

Dosage Form

Strength

200MG

Approval Date

1994-02-14

Regulatory Status

Discontinued

1994

14 Feb

Discontinued Application: 40052

Drug Name

THEOPHYLLINE

Product Number

Dosage Form

Strength

300MG

Approval Date

1994-02-14

40052 / 4 View Details

Active Ingredient

THEOPHYLLINE

Application Number

40052

Product Number

Dosage Form

Strength

300MG

Approval Date

1994-02-14

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 9255

Drug Name

WOLFINA

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-01-01

9255 / 6 View Details

Active Ingredient

RAUWOLFIA SERPENTINA ROOT

Application Number

9255

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 9255

Drug Name

WOLFINA

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

9255 / 8 View Details

Active Ingredient

RAUWOLFIA SERPENTINA ROOT

Application Number

9255

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown

61 total

Discontinued
Unclassified

Official Source

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

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

Drug Name

AMBENYL

Application Number

9319

Product Number

Active Ingredient

BROMODIPHENHYDRAMINE HYDROCHLORIDE; CODEINE PHOSPHATE

Dosage Form

Strength

12.5MG/5ML;10MG/5ML

FDA Approved Drug Data

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