Lannett Company, Inc. Discontinued
FDA Approved Drugs

Lannett Company, Inc. 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 45
Latest Approval Date Jan 20, 2012
Data Source FDA
First Approval Date Jan 01, 1982

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Company Overview

Company

Lannett Company, Inc. Discontinued

Country

U.S.A

Website

Visit Website

customerservice@lannett.com

Social Profiles

Company Snapshot

Lannett Company, Inc. Discontinued

Lannett Company, Inc.13200 Townsend Road Philadelphia, PA 19154

U.S.A

www.lannett.com/ customerservice@lannett.com View on Map

FDA Approved Drug Records ( 45 records )

1984

31 Aug

Discontinued Application: 83901

Drug Name

AMPHETAMINE SULFATE

Product Number

Dosage Form

Strength

5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-08-31

83901 / 1 View Details

Active Ingredient

AMPHETAMINE SULFATE

Application Number

83901

Product Number

Dosage Form

Strength

5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-08-31

Regulatory Status

Discontinued

1984

31 Aug

Discontinued Application: 83901

Drug Name

AMPHETAMINE SULFATE

Product Number

Dosage Form

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-08-31

83901 / 2 View Details

Active Ingredient

AMPHETAMINE SULFATE

Application Number

83901

Product Number

Dosage Form

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-08-31

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84535

Drug Name

BENZYL BENZOATE

Product Number

Dosage Form

Strength

50%

Approval Date

1982-01-01

84535 / 1 View Details

Active Ingredient

BENZYL BENZOATE

Application Number

84535

Product Number

Dosage Form

Strength

50%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84074

Drug Name

BETHANECHOL CHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

84074 / 1 View Details

Active Ingredient

BETHANECHOL CHLORIDE

Application Number

84074

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84702

Drug Name

BETHANECHOL CHLORIDE

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

84702 / 1 View Details

Active Ingredient

BETHANECHOL CHLORIDE

Application Number

84702

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84712

Drug Name

BETHANECHOL CHLORIDE

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

84712 / 1 View Details

Active Ingredient

BETHANECHOL CHLORIDE

Application Number

84712

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85880

Drug Name

BUTALAN

Product Number

Dosage Form

Strength

33.3MG/5ML

Approval Date

1982-01-01

85880 / 1 View Details

Active Ingredient

BUTABARBITAL SODIUM

Application Number

85880

Product Number

Dosage Form

Strength

33.3MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83903

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

83903 / 1 View Details

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

83903

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83903

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

83903 / 3 View Details

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

83903

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85652

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

Dosage Form

Strength

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

Approval Date

1982-01-01

85652 / 1 View Details

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

85652

Product Number

Dosage Form

Strength

15MG **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: 80868

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

80868 / 1 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

80868

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80868

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

80868 / 2 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

80868

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80939

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

12.5MG/5ML

Approval Date

1982-01-01

80939 / 2 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

80939

Product Number

Dosage Form

Strength

12.5MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80816

Drug Name

FOLIC ACID

Product Number

Dosage Form

Strength

1MG

Approval Date

1982-01-01

80816 / 1 View Details

Active Ingredient

FOLIC ACID

Application Number

80816

Product Number

Dosage Form

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83475

Drug Name

GLUTETHIMIDE

Product Number

Dosage Form

Strength

250MG

Approval Date

1982-01-01

83475 / 1 View Details

Active Ingredient

GLUTETHIMIDE

Application Number

83475

Product Number

Dosage Form

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85571

Drug Name

GLUTETHIMIDE

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

85571 / 1 View Details

Active Ingredient

GLUTETHIMIDE

Application Number

85571

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

03 Feb

Discontinued Application: 89243

Drug Name

LANIAZID

Product Number

Dosage Form

Strength

50MG/5ML

Approval Date

1986-02-03

89243 / 1 View Details

Active Ingredient

ISONIAZID

Application Number

89243

Product Number

Dosage Form

Strength

50MG/5ML

Approval Date

1986-02-03

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84578

Drug Name

LANOPHYLLIN

Product Number

Dosage Form

Strength

80MG/15ML

Approval Date

1982-01-01

84578 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

84578

Product Number

Dosage Form

Strength

80MG/15ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985

18 Oct

Discontinued Application: 86986

Drug Name

LANORINAL

Product Number

Dosage Form

Strength

325MG;50MG;40MG

Approval Date

1985-10-18

86986 / 2 View Details

Active Ingredient

ASPIRIN; BUTALBITAL; CAFFEINE

Application Number

86986

Product Number

Dosage Form

Strength

325MG;50MG;40MG

Approval Date

1985-10-18

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80123

Drug Name

LANTRISUL

Product Number

Dosage Form

Strength

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

Approval Date

1982-01-01

80123 / 2 View Details

Active Ingredient

TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE)

Application Number

80123

Product Number

Dosage Form

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

05 Nov

Discontinued Application: 87092

Drug Name

METHYLTESTOSTERONE

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-11-05

87092 / 1 View Details

Active Ingredient

METHYLTESTOSTERONE

Application Number

87092

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-11-05

Regulatory Status

Discontinued

1983

27 Jan

Discontinued Application: 87111

Drug Name

METHYLTESTOSTERONE

Product Number

Dosage Form

Strength

25MG

Approval Date

1983-01-27

87111 / 1 View Details

Active Ingredient

METHYLTESTOSTERONE

Application Number

87111

Product Number

Dosage Form

Strength

25MG

Approval Date

1983-01-27

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 60607

Drug Name

NEOMYCIN SULFATE

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

60607 / 1 View Details

Active Ingredient

NEOMYCIN SULFATE

Application Number

60607

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84393

Drug Name

NITROFURAZONE

Product Number

Dosage Form

Strength

0.2%

Approval Date

1982-01-01

84393 / 1 View Details

Active Ingredient

NITROFURAZONE

Application Number

84393

Product Number

Dosage Form

Strength

0.2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85915

Drug Name

PENTOBARBITAL SODIUM

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-01-01

85915 / 1 View Details

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

85915

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85937

Drug Name

PENTOBARBITAL SODIUM

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

85937 / 1 View Details

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

85937

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80846

Drug Name

PHENETRON

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

80846 / 1 View Details

Active Ingredient

CHLORPHENIRAMINE MALEATE

Application Number

80846

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2005

15 Apr

Discontinued Application: 40555

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

37.5MG

Approval Date

2005-04-15

40555 / 1 View Details

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

40555

Product Number

Dosage Form

Strength

37.5MG

Approval Date

2005-04-15

Regulatory Status

Discontinued

1983

03 Feb

Discontinued Application: 87022

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

30MG

Approval Date

1983-02-03

87022 / 1 View Details

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

87022

Product Number

Dosage Form

Strength

30MG

Approval Date

1983-02-03

Regulatory Status

Discontinued

2012

20 Jan

Discontinued Application: 87022

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

15MG

Approval Date

2012-01-20

87022 / 2 View Details

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

87022

Product Number

Dosage Form

Strength

15MG

Approval Date

2012-01-20

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80963

Drug Name

PIPERAZINE CITRATE

Product Number

Dosage Form

Strength

EQ 500MG BASE/5ML

Approval Date

1982-01-01

80963 / 1 View Details

Active Ingredient

PIPERAZINE CITRATE

Application Number

80963

Product Number

Dosage Form

Strength

EQ 500MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83693

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

Dosage Form

Strength

250MG

Approval Date

1982-01-01

83693 / 1 View Details

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

83693

Product Number

Dosage Form

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84696

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

84696 / 1 View Details

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

84696

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85903

Drug Name

SECOBARBITAL SODIUM

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-01-01

85903 / 1 View Details

Active Ingredient

SECOBARBITAL SODIUM

Application Number

85903

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85909

Drug Name

SECOBARBITAL SODIUM

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

85909 / 1 View Details

Active Ingredient

SECOBARBITAL SODIUM

Application Number

85909

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 10124

Drug Name

SERPALAN

Product Number

Dosage Form

Strength

0.1MG

Approval Date

1982-01-01

10124 / 1 View Details

Active Ingredient

RESERPINE

Application Number

10124

Product Number

Dosage Form

Strength

0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 10124

Drug Name

SERPALAN

Product Number

Dosage Form

Strength

0.25MG

Approval Date

1982-01-01

10124 / 2 View Details

Active Ingredient

RESERPINE

Application Number

10124

Product Number

Dosage Form

Strength

0.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85849

Drug Name

SODIUM BUTABARBITAL

Product Number

Dosage Form

Strength

15MG

Approval Date

1982-01-01

85849 / 1 View Details

Active Ingredient

BUTABARBITAL SODIUM

Application Number

85849

Product Number

Dosage Form

Strength

15MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85866

Drug Name

SODIUM BUTABARBITAL

Product Number

Dosage Form

Strength

30MG

Approval Date

1982-01-01

85866 / 1 View Details

Active Ingredient

BUTABARBITAL SODIUM

Application Number

85866

Product Number

Dosage Form

Strength

30MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85881

Drug Name

SODIUM BUTABARBITAL

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-01-01

85881 / 1 View Details

Active Ingredient

BUTABARBITAL SODIUM

Application Number

85881

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80138

Drug Name

SODIUM P.A.S.

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

80138 / 2 View Details

Active Ingredient

AMINOSALICYLATE SODIUM

Application Number

80138

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80085

Drug Name

SULFISOXAZOLE

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

80085 / 1 View Details

Active Ingredient

SULFISOXAZOLE

Application Number

80085

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83436

Drug Name

TRICHLOREX

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

83436 / 1 View Details

Active Ingredient

TRICHLORMETHIAZIDE

Application Number

83436

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85630

Drug Name

TRICHLOREX

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

85630 / 1 View Details

Active Ingredient

TRICHLORMETHIAZIDE

Application Number

85630

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83557

Drug Name

TRIPELENNAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

83557 / 1 View Details

Active Ingredient

TRIPELENNAMINE HYDROCHLORIDE

Application Number

83557

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown

45 total

Discontinued

Official Source

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

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Drug Name

AMPHETAMINE SULFATE

Application Number

83901

Product Number

Active Ingredient

AMPHETAMINE SULFATE

Dosage Form

Strength

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

FDA Approved Drug Data

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