Lannett Company, Inc.
FDA Approved Drugs

Lannett Company, 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 RX
  • Total Records 67
  • Latest Approval Date Jan 20, 2012
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
67
View
Unclassified
10
View
Discontinued
45
View
RX
12
View
Company Overview

Company

Lannett Company, Inc.

Country

U.S.A

Website

Visit Website

Email

customerservice@lannett.com

Social Profiles

Company Snapshot

Lannett Company, Inc.

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 ( 67 records )
1984
31 Aug
Discontinued Application: 83901

Drug Name

AMPHETAMINE SULFATE

Product Number

1

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5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

Active Ingredient

AMPHETAMINE SULFATE

Application Number

83901

Product Number

1

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5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

2

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10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

Active Ingredient

AMPHETAMINE SULFATE

Application Number

83901

Product Number

2

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10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

1

Dosage Form

-

Strength

50%

Approval Date

1982-01-01

84535 / 1

Active Ingredient

BENZYL BENZOATE

Application Number

84535

Product Number

1

Dosage Form

-

Strength

50%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84074

Drug Name

BETHANECHOL CHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

84074 / 1

Active Ingredient

BETHANECHOL CHLORIDE

Application Number

84074

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84702

Drug Name

BETHANECHOL CHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

84702 / 1

Active Ingredient

BETHANECHOL CHLORIDE

Application Number

84702

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84712

Drug Name

BETHANECHOL CHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

84712 / 1

Active Ingredient

BETHANECHOL CHLORIDE

Application Number

84712

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85880

Drug Name

BUTALAN

Product Number

1

Dosage Form

-

Strength

33.3MG/5ML

Approval Date

1982-01-01

85880 / 1

Active Ingredient

BUTABARBITAL SODIUM

Application Number

85880

Product Number

1

Dosage Form

-

Strength

33.3MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

-
Unclassified Application: 65242

Drug Name

CLINDAMYCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

-

65242 / 1

Active Ingredient

CLINDAMYCIN HYDROCHLORIDE

Application Number

65242

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 65242

Drug Name

CLINDAMYCIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

-

65242 / 2

Active Ingredient

CLINDAMYCIN HYDROCHLORIDE

Application Number

65242

Product Number

2

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78214

Drug Name

DANAZOL

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

78214 / 1

Active Ingredient

DANAZOL

Application Number

78214

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78214

Drug Name

DANAZOL

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

-

78214 / 2

Active Ingredient

DANAZOL

Application Number

78214

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

1982
01 Jan
Discontinued Application: 83903

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

83903 / 1

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

83903

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83903

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

83903 / 3

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

83903

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85652

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

1

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

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

85652

Product Number

1

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

1999
26 Feb
RX Application: 40230

Drug Name

DICYCLOMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1999-02-26

40230 / 1

Active Ingredient

DICYCLOMINE HYDROCHLORIDE

Application Number

40230

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1999-02-26

Regulatory Status

RX

1982
01 Jan
RX Application: 84285

Drug Name

DICYCLOMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

84285 / 1

Active Ingredient

DICYCLOMINE HYDROCHLORIDE

Application Number

84285

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 80868

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

80868 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

80868

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80868

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

80868 / 2

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

80868

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80939

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1982-01-01

80939 / 2

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

80939

Product Number

2

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
RX Application: 85372

Drug Name

DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Product Number

1

Dosage Form

-

Strength

0.025MG;2.5MG

Approval Date

1982-01-01

85372 / 1

Active Ingredient

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Application Number

85372

Product Number

1

Dosage Form

-

Strength

0.025MG;2.5MG

Approval Date

1982-01-01

Regulatory Status

RX

-
Unclassified Application: 89740

Drug Name

FLUPHENAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

-

89740 / 1

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

89740

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 89741

Drug Name

FLUPHENAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

-

89741 / 1

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

89741

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 89742

Drug Name

FLUPHENAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

-

89742 / 1

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

89742

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

-

Regulatory Status

Unclassified

1982
01 Jan
Discontinued Application: 80816

Drug Name

FOLIC ACID

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

80816 / 1

Active Ingredient

FOLIC ACID

Application Number

80816

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83475

Drug Name

GLUTETHIMIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

83475 / 1

Active Ingredient

GLUTETHIMIDE

Application Number

83475

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85571

Drug Name

GLUTETHIMIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

85571 / 1

Active Ingredient

GLUTETHIMIDE

Application Number

85571

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

-
Unclassified Application: 78439

Drug Name

HYDROMORPHONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

-

78439 / 1

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

78439

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78439

Drug Name

HYDROMORPHONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

-

78439 / 2

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

78439

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

-

Regulatory Status

Unclassified

1986
03 Feb
Discontinued Application: 89243

Drug Name

LANIAZID

Product Number

1

Dosage Form

-

Strength

50MG/5ML

Approval Date

1986-02-03

89243 / 1

Active Ingredient

ISONIAZID

Application Number

89243

Product Number

1

Dosage Form

-

Strength

50MG/5ML

Approval Date

1986-02-03

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84578

Drug Name

LANOPHYLLIN

Product Number

1

Dosage Form

-

Strength

80MG/15ML

Approval Date

1982-01-01

84578 / 1

Active Ingredient

THEOPHYLLINE

Application Number

84578

Product Number

1

Dosage Form

-

Strength

80MG/15ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
18 Oct
Discontinued Application: 86986

Drug Name

LANORINAL

Product Number

2

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-10-18

86986 / 2

Active Ingredient

ASPIRIN; BUTALBITAL; CAFFEINE

Application Number

86986

Product Number

2

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

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

80123 / 2

Active Ingredient

TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE)

Application Number

80123

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

2001
03 Apr
RX Application: 21259

Drug Name

METADATE CD

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2001-04-03

21259 / 1

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2001-04-03

Regulatory Status

RX

2003
19 Jun
RX Application: 21259

Drug Name

METADATE CD

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2003-06-19

21259 / 2

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2003-06-19

Regulatory Status

RX

2003
27 May
RX Application: 21259

Drug Name

METADATE CD

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2003-05-27

21259 / 3

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2003-05-27

Regulatory Status

RX

2006
19 Feb
RX Application: 21259

Drug Name

METADATE CD

Product Number

4

Dosage Form

-

Strength

40MG

Approval Date

2006-02-19

21259 / 4

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

4

Dosage Form

-

Strength

40MG

Approval Date

2006-02-19

Regulatory Status

RX

2006
19 Feb
RX Application: 21259

Drug Name

METADATE CD

Product Number

5

Dosage Form

-

Strength

50MG

Approval Date

2006-02-19

21259 / 5

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

5

Dosage Form

-

Strength

50MG

Approval Date

2006-02-19

Regulatory Status

RX

2006
19 Feb
RX Application: 21259

Drug Name

METADATE CD

Product Number

6

Dosage Form

-

Strength

60MG

Approval Date

2006-02-19

21259 / 6

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

6

Dosage Form

-

Strength

60MG

Approval Date

2006-02-19

Regulatory Status

RX

1982
05 Nov
Discontinued Application: 87092

Drug Name

METHYLTESTOSTERONE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-11-05

87092 / 1

Active Ingredient

METHYLTESTOSTERONE

Application Number

87092

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-11-05

Regulatory Status

Discontinued

1983
27 Jan
Discontinued Application: 87111

Drug Name

METHYLTESTOSTERONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-01-27

87111 / 1

Active Ingredient

METHYLTESTOSTERONE

Application Number

87111

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-01-27

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60607

Drug Name

NEOMYCIN SULFATE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

60607 / 1

Active Ingredient

NEOMYCIN SULFATE

Application Number

60607

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84393

Drug Name

NITROFURAZONE

Product Number

1

Dosage Form

-

Strength

0.2%

Approval Date

1982-01-01

84393 / 1

Active Ingredient

NITROFURAZONE

Application Number

84393

Product Number

1

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

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

85915 / 1

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

85915

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85937

Drug Name

PENTOBARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

85937 / 1

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

85937

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80846

Drug Name

PHENETRON

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

80846 / 1

Active Ingredient

CHLORPHENIRAMINE MALEATE

Application Number

80846

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2005
15 Apr
Discontinued Application: 40555

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

2005-04-15

40555 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

40555

Product Number

1

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

1

Dosage Form

-

Strength

30MG

Approval Date

1983-02-03

87022 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

87022

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1983-02-03

Regulatory Status

Discontinued

2012
20 Jan
Discontinued Application: 87022

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2012-01-20

87022 / 2

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

87022

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2012-01-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80963

Drug Name

PIPERAZINE CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/5ML

Approval Date

1982-01-01

80963 / 1

Active Ingredient

PIPERAZINE CITRATE

Application Number

80963

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
RX Application: 84903

Drug Name

PRIMIDONE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

84903 / 1

Active Ingredient

PRIMIDONE

Application Number

84903

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

RX

2001
24 May
RX Application: 84903

Drug Name

PRIMIDONE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2001-05-24

84903 / 2

Active Ingredient

PRIMIDONE

Application Number

84903

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2001-05-24

Regulatory Status

RX

1982
01 Jan
RX Application: 80966

Drug Name

PROBALAN

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

80966 / 1

Active Ingredient

PROBENECID

Application Number

80966

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 83693

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

83693 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

83693

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84696

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

84696 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

84696

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85903

Drug Name

SECOBARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

85903 / 1

Active Ingredient

SECOBARBITAL SODIUM

Application Number

85903

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85909

Drug Name

SECOBARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

85909 / 1

Active Ingredient

SECOBARBITAL SODIUM

Application Number

85909

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 10124

Drug Name

SERPALAN

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

10124 / 1

Active Ingredient

RESERPINE

Application Number

10124

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 10124

Drug Name

SERPALAN

Product Number

2

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

10124 / 2

Active Ingredient

RESERPINE

Application Number

10124

Product Number

2

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

1

Dosage Form

-

Strength

15MG

Approval Date

1982-01-01

85849 / 1

Active Ingredient

BUTABARBITAL SODIUM

Application Number

85849

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85866

Drug Name

SODIUM BUTABARBITAL

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1982-01-01

85866 / 1

Active Ingredient

BUTABARBITAL SODIUM

Application Number

85866

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85881

Drug Name

SODIUM BUTABARBITAL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

85881 / 1

Active Ingredient

BUTABARBITAL SODIUM

Application Number

85881

Product Number

1

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

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

80138 / 2

Active Ingredient

AMINOSALICYLATE SODIUM

Application Number

80138

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80085

Drug Name

SULFISOXAZOLE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

80085 / 1

Active Ingredient

SULFISOXAZOLE

Application Number

80085

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83436

Drug Name

TRICHLOREX

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

83436 / 1

Active Ingredient

TRICHLORMETHIAZIDE

Application Number

83436

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85630

Drug Name

TRICHLOREX

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

85630 / 1

Active Ingredient

TRICHLORMETHIAZIDE

Application Number

85630

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83557

Drug Name

TRIPELENNAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

83557 / 1

Active Ingredient

TRIPELENNAMINE HYDROCHLORIDE

Application Number

83557

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

-
Unclassified Application: 84088

Drug Name

VELTANE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

-

84088 / 1

Active Ingredient

BROMPHENIRAMINE MALEATE

Application Number

84088

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

-

Regulatory Status

Unclassified

Related Databases
  • FDA Inspections
    14 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    67 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
67 total
  • Discontinued
  • Unclassified
  • RX
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

AMPHETAMINE SULFATE

Application Number

83901

Product Number

1

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

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit