Apothecon Pharmaceuticals
FDA Approved Drugs

Apothecon Pharmaceuticals

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 RX
  • Total Records 246
  • Latest Approval Date Apr 12, 2019
  • Data Source FDA
  • First Approval Date Jan 01, 1982
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Discontinued
243
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Company Overview

Company

Apothecon Pharmaceuticals

Country

India

Website

Visit Website

Email

rahul.verma@apotheconpharma.com

Social Profiles

LinkedIn
Company Snapshot

Apothecon Pharmaceuticals

Padra – Jambusar Highway, P.O. – Dabhasa, Pin – 391 440, Ta. Padra, Dist. Vadodara, Gujarat

India

www.apotheconpharma.com/ rahul.verma@apotheconpharma.com View on Map
FDA Approved Drug Records ( 246 records )
1998
27 Feb
Discontinued Application: 74897

Drug Name

ACYCLOVIR SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1998-02-27

74897 / 1

Active Ingredient

ACYCLOVIR SODIUM

Application Number

74897

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1998-02-27

Regulatory Status

Discontinued

1998
27 Feb
Discontinued Application: 74897

Drug Name

ACYCLOVIR SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1998-02-27

74897 / 2

Active Ingredient

ACYCLOVIR SODIUM

Application Number

74897

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1998-02-27

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50495

Drug Name

AMIKIN

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50495 / 1

Active Ingredient

AMIKACIN SULFATE

Application Number

50495

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50495

Drug Name

AMIKIN

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50495 / 2

Active Ingredient

AMIKACIN SULFATE

Application Number

50495

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62311

Drug Name

AMIKIN

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/ML

Approval Date

1982-01-01

62311 / 1

Active Ingredient

AMIKACIN SULFATE

Application Number

62311

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62311

Drug Name

AMIKIN

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/ML

Approval Date

1982-01-01

62311 / 2

Active Ingredient

AMIKACIN SULFATE

Application Number

62311

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
20 Sep
Discontinued Application: 62562

Drug Name

AMIKIN

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/ML

Approval Date

1984-09-20

62562 / 1

Active Ingredient

AMIKACIN SULFATE

Application Number

62562

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/ML

Approval Date

1984-09-20

Regulatory Status

Discontinued

1984
20 Sep
Discontinued Application: 62562

Drug Name

AMIKIN

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/ML

Approval Date

1984-09-20

62562 / 2

Active Ingredient

AMIKACIN SULFATE

Application Number

62562

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/ML

Approval Date

1984-09-20

Regulatory Status

Discontinued

1987
30 Nov
Discontinued Application: 50618

Drug Name

AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

1987-11-30

50618 / 1

Active Ingredient

AMIKACIN SULFATE

Application Number

50618

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

1987-11-30

Regulatory Status

Discontinued

1987
30 Nov
Discontinued Application: 50618

Drug Name

AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

1987-11-30

50618 / 2

Active Ingredient

AMIKACIN SULFATE

Application Number

50618

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

1987-11-30

Regulatory Status

Discontinued

1996
06 May
Discontinued Application: 64131

Drug Name

AMOXICILLIN

Product Number

1

Dosage Form

-

Strength

125MG

Approval Date

1996-05-06

64131 / 1

Active Ingredient

AMOXICILLIN

Application Number

64131

Product Number

1

Dosage Form

-

Strength

125MG

Approval Date

1996-05-06

Regulatory Status

Discontinued

1996
06 May
Discontinued Application: 64131

Drug Name

AMOXICILLIN

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

1996-05-06

64131 / 2

Active Ingredient

AMOXICILLIN

Application Number

64131

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

1996-05-06

Regulatory Status

Discontinued

1988
05 Feb
Discontinued Application: 62860

Drug Name

AMPICILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1988-02-05

62860 / 1

Active Ingredient

AMPICILLIN SODIUM

Application Number

62860

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1988-02-05

Regulatory Status

Discontinued

1988
05 Feb
Discontinued Application: 62860

Drug Name

AMPICILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1988-02-05

62860 / 2

Active Ingredient

AMPICILLIN SODIUM

Application Number

62860

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1988-02-05

Regulatory Status

Discontinued

1988
05 Feb
Discontinued Application: 62860

Drug Name

AMPICILLIN SODIUM

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1988-02-05

62860 / 3

Active Ingredient

AMPICILLIN SODIUM

Application Number

62860

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1988-02-05

Regulatory Status

Discontinued

1988
05 Feb
Discontinued Application: 62860

Drug Name

AMPICILLIN SODIUM

Product Number

4

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1988-02-05

62860 / 4

Active Ingredient

AMPICILLIN SODIUM

Application Number

62860

Product Number

4

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1988-02-05

Regulatory Status

Discontinued

1988
05 Feb
Discontinued Application: 62860

Drug Name

AMPICILLIN SODIUM

Product Number

5

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1988-02-05

62860 / 5

Active Ingredient

AMPICILLIN SODIUM

Application Number

62860

Product Number

5

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1988-02-05

Regulatory Status

Discontinued

1992
20 Mar
Discontinued Application: 73317

Drug Name

ATENOLOL

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1992-03-20

73317 / 1

Active Ingredient

ATENOLOL

Application Number

73317

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1992-03-20

Regulatory Status

Discontinued

1992
20 Mar
Discontinued Application: 73318

Drug Name

ATENOLOL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1992-03-20

73318 / 1

Active Ingredient

ATENOLOL

Application Number

73318

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1992-03-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61149

Drug Name

BETAPEN-VK

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

61149 / 1

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61149

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61149

Drug Name

BETAPEN-VK

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

61149 / 2

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61149

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

2000
27 Dec
Discontinued Application: 75642

Drug Name

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

5MG;6.25MG

Approval Date

2000-12-27

75642 / 1

Active Ingredient

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Application Number

75642

Product Number

1

Dosage Form

-

Strength

5MG;6.25MG

Approval Date

2000-12-27

Regulatory Status

Discontinued

2000
27 Dec
Discontinued Application: 75642

Drug Name

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

2.5MG;6.25MG

Approval Date

2000-12-27

75642 / 2

Active Ingredient

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Application Number

75642

Product Number

2

Dosage Form

-

Strength

2.5MG;6.25MG

Approval Date

2000-12-27

Regulatory Status

Discontinued

2000
27 Dec
Discontinued Application: 75642

Drug Name

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

10MG;6.25MG

Approval Date

2000-12-27

75642 / 3

Active Ingredient

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Application Number

75642

Product Number

3

Dosage Form

-

Strength

10MG;6.25MG

Approval Date

2000-12-27

Regulatory Status

Discontinued

1984
12 Oct
Discontinued Application: 18709

Drug Name

CAPOZIDE 25/15

Product Number

1

Dosage Form

-

Strength

25MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-10-12

18709 / 1

Active Ingredient

CAPTOPRIL; HYDROCHLOROTHIAZIDE

Application Number

18709

Product Number

1

Dosage Form

-

Strength

25MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-10-12

Regulatory Status

Discontinued

1984
12 Oct
Discontinued Application: 18709

Drug Name

CAPOZIDE 25/25

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1984-10-12

18709 / 2

Active Ingredient

CAPTOPRIL; HYDROCHLOROTHIAZIDE

Application Number

18709

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1984-10-12

Regulatory Status

Discontinued

1984
12 Oct
Discontinued Application: 18709

Drug Name

CAPOZIDE 50/15

Product Number

4

Dosage Form

-

Strength

50MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-10-12

18709 / 4

Active Ingredient

CAPTOPRIL; HYDROCHLOROTHIAZIDE

Application Number

18709

Product Number

4

Dosage Form

-

Strength

50MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-10-12

Regulatory Status

Discontinued

1984
12 Oct
Discontinued Application: 18709

Drug Name

CAPOZIDE 50/25

Product Number

3

Dosage Form

-

Strength

50MG;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-10-12

18709 / 3

Active Ingredient

CAPTOPRIL; HYDROCHLOROTHIAZIDE

Application Number

18709

Product Number

3

Dosage Form

-

Strength

50MG;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-10-12

Regulatory Status

Discontinued

1995
31 Mar
Discontinued Application: 74472

Drug Name

CAPTOPRIL

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

1995-03-31

74472 / 1

Active Ingredient

CAPTOPRIL

Application Number

74472

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

1995-03-31

Regulatory Status

Discontinued

1995
31 Mar
Discontinued Application: 74472

Drug Name

CAPTOPRIL

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1995-03-31

74472 / 2

Active Ingredient

CAPTOPRIL

Application Number

74472

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1995-03-31

Regulatory Status

Discontinued

1995
31 Mar
Discontinued Application: 74472

Drug Name

CAPTOPRIL

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1995-03-31

74472 / 3

Active Ingredient

CAPTOPRIL

Application Number

74472

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1995-03-31

Regulatory Status

Discontinued

1995
31 Mar
Discontinued Application: 74472

Drug Name

CAPTOPRIL

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

1995-03-31

74472 / 4

Active Ingredient

CAPTOPRIL

Application Number

74472

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

1995-03-31

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62334

Drug Name

CEFADROXIL

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

62334 / 1

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

62334

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62334

Drug Name

CEFADROXIL

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

62334 / 2

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

62334

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62334

Drug Name

CEFADROXIL

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE/5ML

Approval Date

1982-01-01

62334 / 3

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

62334

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50446

Drug Name

CEFADYL

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

50446 / 1

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

50446

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50446

Drug Name

CEFADYL

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1982-01-01

50446 / 2

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

50446

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50446

Drug Name

CEFADYL

Product Number

3

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

1982-01-01

50446 / 3

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

50446

Product Number

3

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50446

Drug Name

CEFADYL

Product Number

4

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

1982-01-01

50446 / 4

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

50446

Product Number

4

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50446

Drug Name

CEFADYL

Product Number

5

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1982-01-01

50446 / 5

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

50446

Product Number

5

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61769

Drug Name

CEFADYL

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

61769 / 1

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

61769

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61769

Drug Name

CEFADYL

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1982-01-01

61769 / 2

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

61769

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61769

Drug Name

CEFADYL

Product Number

3

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

1982-01-01

61769 / 3

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

61769

Product Number

3

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
23 Dec
Discontinued Application: 62724

Drug Name

CEFADYL

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-12-23

62724 / 1

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62724

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-12-23

Regulatory Status

Discontinued

1986
23 Dec
Discontinued Application: 62724

Drug Name

CEFADYL

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1986-12-23

62724 / 2

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62724

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1986-12-23

Regulatory Status

Discontinued

1988
20 Sep
Discontinued Application: 62961

Drug Name

CEFADYL

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1988-09-20

62961 / 1

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62961

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1988-09-20

Regulatory Status

Discontinued

1988
20 Sep
Discontinued Application: 62961

Drug Name

CEFADYL

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1988-09-20

62961 / 2

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62961

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1988-09-20

Regulatory Status

Discontinued

1988
20 Sep
Discontinued Application: 62961

Drug Name

CEFADYL

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1988-09-20

62961 / 3

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62961

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1988-09-20

Regulatory Status

Discontinued

1988
20 Sep
Discontinued Application: 62961

Drug Name

CEFADYL

Product Number

4

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

1988-09-20

62961 / 4

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62961

Product Number

4

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

1988-09-20

Regulatory Status

Discontinued

1988
08 Nov
Discontinued Application: 62973

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1988-11-08

62973 / 1

Active Ingredient

CEPHALEXIN

Application Number

62973

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1988-11-08

Regulatory Status

Discontinued

1988
23 Nov
Discontinued Application: 62974

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1988-11-23

62974 / 1

Active Ingredient

CEPHALEXIN

Application Number

62974

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1988-11-23

Regulatory Status

Discontinued

1991
18 Apr
Discontinued Application: 62986

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1991-04-18

62986 / 1

Active Ingredient

CEPHALEXIN

Application Number

62986

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1991-04-18

Regulatory Status

Discontinued

1989
25 Jul
Discontinued Application: 62987

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1989-07-25

62987 / 1

Active Ingredient

CEPHALEXIN

Application Number

62987

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1989-07-25

Regulatory Status

Discontinued

1989
29 Sep
Discontinued Application: 63063

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1989-09-29

63063 / 1

Active Ingredient

CEPHALEXIN

Application Number

63063

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1989-09-29

Regulatory Status

Discontinued

1989
29 Sep
Discontinued Application: 63063

Drug Name

CEPHALEXIN

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1989-09-29

63063 / 2

Active Ingredient

CEPHALEXIN

Application Number

63063

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1989-09-29

Regulatory Status

Discontinued

1994
30 Dec
Discontinued Application: 63186

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1994-12-30

63186 / 1

Active Ingredient

CEPHALEXIN

Application Number

63186

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1994-12-30

Regulatory Status

Discontinued

1994
30 Dec
Discontinued Application: 63186

Drug Name

CEPHALEXIN

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1994-12-30

63186 / 2

Active Ingredient

CEPHALEXIN

Application Number

63186

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1994-12-30

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61452

Drug Name

CLOXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

61452 / 1

Active Ingredient

CLOXACILLIN SODIUM

Application Number

61452

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61452

Drug Name

CLOXACILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

61452 / 2

Active Ingredient

CLOXACILLIN SODIUM

Application Number

61452

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61455

Drug Name

DICLOXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 62.5MG BASE/5ML

Approval Date

1982-01-01

61455 / 1

Active Ingredient

DICLOXACILLIN SODIUM

Application Number

61455

Product Number

1

Dosage Form

-

Strength

EQ 62.5MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993
31 Mar
Discontinued Application: 74051

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1993-03-31

74051 / 1

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

74051

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1993-03-31

Regulatory Status

Discontinued

1993
31 Mar
Discontinued Application: 74051

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

1993-03-31

74051 / 2

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

74051

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

1993-03-31

Regulatory Status

Discontinued

1993
31 Mar
Discontinued Application: 74051

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

90MG

Approval Date

1993-03-31

74051 / 3

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

74051

Product Number

3

Dosage Form

-

Strength

90MG

Approval Date

1993-03-31

Regulatory Status

Discontinued

1993
31 Mar
Discontinued Application: 74051

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

120MG

Approval Date

1993-03-31

74051 / 4

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

74051

Product Number

4

Dosage Form

-

Strength

120MG

Approval Date

1993-03-31

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50337

Drug Name

DYNAPEN

Product Number

2

Dosage Form

-

Strength

EQ 62.5MG BASE/5ML

Approval Date

1982-01-01

50337 / 2

Active Ingredient

DICLOXACILLIN SODIUM

Application Number

50337

Product Number

2

Dosage Form

-

Strength

EQ 62.5MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

2000
22 Aug
Discontinued Application: 75583

Drug Name

ENALAPRIL MALEATE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2000-08-22

75583 / 1

Active Ingredient

ENALAPRIL MALEATE

Application Number

75583

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2000-08-22

Regulatory Status

Discontinued

2000
22 Aug
Discontinued Application: 75583

Drug Name

ENALAPRIL MALEATE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2000-08-22

75583 / 2

Active Ingredient

ENALAPRIL MALEATE

Application Number

75583

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2000-08-22

Regulatory Status

Discontinued

2000
22 Aug
Discontinued Application: 75583

Drug Name

ENALAPRIL MALEATE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2000-08-22

75583 / 3

Active Ingredient

ENALAPRIL MALEATE

Application Number

75583

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2000-08-22

Regulatory Status

Discontinued

2000
22 Aug
Discontinued Application: 75583

Drug Name

ENALAPRIL MALEATE

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2000-08-22

75583 / 4

Active Ingredient

ENALAPRIL MALEATE

Application Number

75583

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2000-08-22

Regulatory Status

Discontinued

2001
16 Apr
Discontinued Application: 75707

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

2001-04-16

75707 / 1

Active Ingredient

FAMOTIDINE

Application Number

75707

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

2001-04-16

Regulatory Status

Discontinued

2001
16 Apr
Discontinued Application: 75708

Drug Name

FAMOTIDINE PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

2001-04-16

75708 / 1

Active Ingredient

FAMOTIDINE

Application Number

75708

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

2001-04-16

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50313

Drug Name

FUNGIZONE

Product Number

1

Dosage Form

-

Strength

3%

Approval Date

1982-01-01

50313 / 1

Active Ingredient

AMPHOTERICIN B

Application Number

50313

Product Number

1

Dosage Form

-

Strength

3%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50314

Drug Name

FUNGIZONE

Product Number

1

Dosage Form

-

Strength

3%

Approval Date

1982-01-01

50314 / 1

Active Ingredient

AMPHOTERICIN B

Application Number

50314

Product Number

1

Dosage Form

-

Strength

3%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60517

Drug Name

FUNGIZONE

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1982-01-01

60517 / 1

Active Ingredient

AMPHOTERICIN B

Application Number

60517

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60570

Drug Name

FUNGIZONE

Product Number

1

Dosage Form

-

Strength

3%

Approval Date

1982-01-01

60570 / 1

Active Ingredient

AMPHOTERICIN B

Application Number

60570

Product Number

1

Dosage Form

-

Strength

3%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60516

Drug Name

KANTREX

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

60516 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

60516

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61655

Drug Name

KANTREX

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/2ML

Approval Date

1982-01-01

61655 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

61655

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/2ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61655

Drug Name

KANTREX

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1982-01-01

61655 / 2

Active Ingredient

KANAMYCIN SULFATE

Application Number

61655

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61655

Drug Name

KANTREX

Product Number

3

Dosage Form

-

Strength

EQ 75MG BASE/2ML

Approval Date

1982-01-01

61655 / 3

Active Ingredient

KANAMYCIN SULFATE

Application Number

61655

Product Number

3

Dosage Form

-

Strength

EQ 75MG BASE/2ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61901

Drug Name

KANTREX

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/2ML

Approval Date

1982-01-01

61901 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

61901

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/2ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61901

Drug Name

KANTREX

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1982-01-01

61901 / 2

Active Ingredient

KANAMYCIN SULFATE

Application Number

61901

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61901

Drug Name

KANTREX

Product Number

3

Dosage Form

-

Strength

EQ 75MG BASE/2ML

Approval Date

1982-01-01

61901 / 3

Active Ingredient

KANAMYCIN SULFATE

Application Number

61901

Product Number

3

Dosage Form

-

Strength

EQ 75MG BASE/2ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61911

Drug Name

KANTREX

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

61911 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

61911

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
21 Sep
Discontinued Application: 62564

Drug Name

KANTREX

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE/2ML

Approval Date

1984-09-21

62564 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

62564

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE/2ML

Approval Date

1984-09-21

Regulatory Status

Discontinued

1984
21 Sep
Discontinued Application: 62564

Drug Name

KANTREX

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/2ML

Approval Date

1984-09-21

62564 / 2

Active Ingredient

KANAMYCIN SULFATE

Application Number

62564

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/2ML

Approval Date

1984-09-21

Regulatory Status

Discontinued

1984
21 Sep
Discontinued Application: 62564

Drug Name

KANTREX

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1984-09-21

62564 / 3

Active Ingredient

KANAMYCIN SULFATE

Application Number

62564

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1984-09-21

Regulatory Status

Discontinued

1987
06 Mar
Discontinued Application: 62726

Drug Name

KANTREX

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1987-03-06

62726 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

62726

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1987-03-06

Regulatory Status

Discontinued

1982
01 Jan
RX Application: 12041

Drug Name

KENALOG-10

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1982-01-01

12041 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

12041

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 14901

Drug Name

KENALOG-40

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1982-01-01

14901 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

14901

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1982-01-01

Regulatory Status

RX

2019
12 Apr
RX Application: 14901

Drug Name

KENALOG-80

Product Number

2

Dosage Form

-

Strength

80MG/ML

Approval Date

2019-04-12

14901 / 2

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

14901

Product Number

2

Dosage Form

-

Strength

80MG/ML

Approval Date

2019-04-12

Regulatory Status

RX

2000
28 Nov
Discontinued Application: 75348

Drug Name

KETOROLAC TROMETHAMINE

Product Number

1

Dosage Form

-

Strength

15MG/ML

Approval Date

2000-11-28

75348 / 1

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

75348

Product Number

1

Dosage Form

-

Strength

15MG/ML

Approval Date

2000-11-28

Regulatory Status

Discontinued

2000
28 Nov
Discontinued Application: 75348

Drug Name

KETOROLAC TROMETHAMINE

Product Number

2

Dosage Form

-

Strength

30MG/ML

Approval Date

2000-11-28

75348 / 2

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

75348

Product Number

2

Dosage Form

-

Strength

30MG/ML

Approval Date

2000-11-28

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17850

Drug Name

KLOTRIX

Product Number

1

Dosage Form

-

Strength

10MEQ

Approval Date

1982-01-01

17850 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

17850

Product Number

1

Dosage Form

-

Strength

10MEQ

Approval Date

1982-01-01

Regulatory Status

Discontinued

1998
20 Nov
Discontinued Application: 75223

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1998-11-20

75223 / 1

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

75223

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1998-11-20

Regulatory Status

Discontinued

1998
20 Nov
Discontinued Application: 75223

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

1998-11-20

75223 / 2

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

75223

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

1998-11-20

Regulatory Status

Discontinued

1998
20 Nov
Discontinued Application: 75223

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

1998-11-20

75223 / 3

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

75223

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

1998-11-20

Regulatory Status

Discontinued

1999
29 Nov
Discontinued Application: 75355

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1999-11-29

75355 / 1

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

75355

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1999-11-29

Regulatory Status

Discontinued

1994
27 Jan
Discontinued Application: 74258

Drug Name

METOPROLOL TARTRATE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1994-01-27

74258 / 1

Active Ingredient

METOPROLOL TARTRATE

Application Number

74258

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1994-01-27

Regulatory Status

Discontinued

1994
27 Jan
Discontinued Application: 74258

Drug Name

METOPROLOL TARTRATE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1994-01-27

74258 / 2

Active Ingredient

METOPROLOL TARTRATE

Application Number

74258

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1994-01-27

Regulatory Status

Discontinued

2000
01 Nov
Discontinued Application: 75620

Drug Name

MIDAZOLAM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/ML

Approval Date

2000-11-01

75620 / 1

Active Ingredient

MIDAZOLAM HYDROCHLORIDE

Application Number

75620

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/ML

Approval Date

2000-11-01

Regulatory Status

Discontinued

2000
01 Nov
Discontinued Application: 75620

Drug Name

MIDAZOLAM HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

2000-11-01

75620 / 2

Active Ingredient

MIDAZOLAM HYDROCHLORIDE

Application Number

75620

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

2000-11-01

Regulatory Status

Discontinued

2000
19 Oct
Discontinued Application: 75641

Drug Name

MIDAZOLAM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

2000-10-19

75641 / 1

Active Ingredient

MIDAZOLAM HYDROCHLORIDE

Application Number

75641

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

2000-10-19

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 13601

Drug Name

MUCOMYST

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

13601 / 1

Active Ingredient

ACETYLCYSTEINE

Application Number

13601

Product Number

1

Dosage Form

-

Strength

20% **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: 13601

Drug Name

MUCOMYST

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

13601 / 2

Active Ingredient

ACETYLCYSTEINE

Application Number

13601

Product Number

2

Dosage Form

-

Strength

10% **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: 61984

Drug Name

NAFCILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1982-01-01

61984 / 1

Active Ingredient

NAFCILLIN SODIUM

Application Number

61984

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61984

Drug Name

NAFCILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

61984 / 2

Active Ingredient

NAFCILLIN SODIUM

Application Number

61984

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61984

Drug Name

NAFCILLIN SODIUM

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1982-01-01

61984 / 3

Active Ingredient

NAFCILLIN SODIUM

Application Number

61984

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61984

Drug Name

NAFCILLIN SODIUM

Product Number

5

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

1982-01-01

61984 / 5

Active Ingredient

NAFCILLIN SODIUM

Application Number

61984

Product Number

5

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 12164

Drug Name

NATURETIN-10

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

12164 / 3

Active Ingredient

BENDROFLUMETHIAZIDE

Application Number

12164

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 12164

Drug Name

NATURETIN-2.5

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

12164 / 1

Active Ingredient

BENDROFLUMETHIAZIDE

Application Number

12164

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 12164

Drug Name

NATURETIN-5

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

12164 / 2

Active Ingredient

BENDROFLUMETHIAZIDE

Application Number

12164

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 8883

Drug Name

OPHTHAINE

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

8883 / 1

Active Ingredient

PROPARACAINE HYDROCHLORIDE

Application Number

8883

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50195

Drug Name

OXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

50195 / 1

Active Ingredient

OXACILLIN SODIUM

Application Number

50195

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50195

Drug Name

OXACILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

50195 / 2

Active Ingredient

OXACILLIN SODIUM

Application Number

50195

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50195

Drug Name

OXACILLIN SODIUM

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1982-01-01

50195 / 3

Active Ingredient

OXACILLIN SODIUM

Application Number

50195

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50195

Drug Name

OXACILLIN SODIUM

Product Number

4

Dosage Form

-

Strength

EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50195 / 4

Active Ingredient

OXACILLIN SODIUM

Application Number

50195

Product Number

4

Dosage Form

-

Strength

EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50195

Drug Name

OXACILLIN SODIUM

Product Number

5

Dosage Form

-

Strength

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

Approval Date

1982-01-01

50195 / 5

Active Ingredient

OXACILLIN SODIUM

Application Number

50195

Product Number

5

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61450

Drug Name

OXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

61450 / 1

Active Ingredient

OXACILLIN SODIUM

Application Number

61450

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61450

Drug Name

OXACILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

61450 / 2

Active Ingredient

OXACILLIN SODIUM

Application Number

61450

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61457

Drug Name

OXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

61457 / 1

Active Ingredient

OXACILLIN SODIUM

Application Number

61457

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60362

Drug Name

PENICILLIN G POTASSIUM

Product Number

1

Dosage Form

-

Strength

1,000,000 UNITS/VIAL

Approval Date

1982-01-01

60362 / 1

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60362

Product Number

1

Dosage Form

-

Strength

1,000,000 UNITS/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60362

Drug Name

PENICILLIN G POTASSIUM

Product Number

2

Dosage Form

-

Strength

20,000,000 UNITS/VIAL

Approval Date

1982-01-01

60362 / 2

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60362

Product Number

2

Dosage Form

-

Strength

20,000,000 UNITS/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60362

Drug Name

PENICILLIN G POTASSIUM

Product Number

3

Dosage Form

-

Strength

5,000,000 UNITS/VIAL

Approval Date

1982-01-01

60362 / 3

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60362

Product Number

3

Dosage Form

-

Strength

5,000,000 UNITS/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60362

Drug Name

PENICILLIN G POTASSIUM

Product Number

4

Dosage Form

-

Strength

10,000,000 UNITS/VIAL

Approval Date

1982-01-01

60362 / 4

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60362

Product Number

4

Dosage Form

-

Strength

10,000,000 UNITS/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60392

Drug Name

PENICILLIN G POTASSIUM

Product Number

3

Dosage Form

-

Strength

250,000 UNITS

Approval Date

1982-01-01

60392 / 3

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60392

Product Number

3

Dosage Form

-

Strength

250,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62149

Drug Name

PENTIDS 200

Product Number

1

Dosage Form

-

Strength

200,000 UNITS/5ML

Approval Date

1982-01-01

62149 / 1

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

62149

Product Number

1

Dosage Form

-

Strength

200,000 UNITS/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62155

Drug Name

PENTIDS 200

Product Number

1

Dosage Form

-

Strength

200,000 UNITS

Approval Date

1982-01-01

62155 / 1

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

62155

Product Number

1

Dosage Form

-

Strength

200,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62155

Drug Name

PENTIDS 250

Product Number

2

Dosage Form

-

Strength

250,000 UNITS

Approval Date

1982-01-01

62155 / 2

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

62155

Product Number

2

Dosage Form

-

Strength

250,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60392

Drug Name

PENTIDS 400

Product Number

4

Dosage Form

-

Strength

400,000 UNITS

Approval Date

1982-01-01

60392 / 4

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60392

Product Number

4

Dosage Form

-

Strength

400,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62149

Drug Name

PENTIDS 400

Product Number

2

Dosage Form

-

Strength

400,000 UNITS/5ML

Approval Date

1982-01-01

62149 / 2

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

62149

Product Number

2

Dosage Form

-

Strength

400,000 UNITS/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62155

Drug Name

PENTIDS 400

Product Number

3

Dosage Form

-

Strength

400,000 UNITS

Approval Date

1982-01-01

62155 / 3

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

62155

Product Number

3

Dosage Form

-

Strength

400,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60392

Drug Name

PENTIDS 800

Product Number

5

Dosage Form

-

Strength

800,000 UNITS

Approval Date

1982-01-01

60392 / 5

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

60392

Product Number

5

Dosage Form

-

Strength

800,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62155

Drug Name

PENTIDS 800

Product Number

4

Dosage Form

-

Strength

800,000 UNITS

Approval Date

1982-01-01

62155 / 4

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

62155

Product Number

4

Dosage Form

-

Strength

800,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62297

Drug Name

POLYCILLIN

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

62297 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

62297

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62297

Drug Name

POLYCILLIN

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

62297 / 2

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

62297

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61898

Drug Name

POLYCILLIN-PRB

Product Number

1

Dosage Form

-

Strength

EQ 3.5GM BASE/BOT;1GM/BOT

Approval Date

1982-01-01

61898 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE; PROBENECID

Application Number

61898

Product Number

1

Dosage Form

-

Strength

EQ 3.5GM BASE/BOT;1GM/BOT

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61851

Drug Name

POLYMOX

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

61851 / 1

Active Ingredient

AMOXICILLIN

Application Number

61851

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61851

Drug Name

POLYMOX

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

61851 / 2

Active Ingredient

AMOXICILLIN

Application Number

61851

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62323

Drug Name

POLYMOX

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

62323 / 1

Active Ingredient

AMOXICILLIN

Application Number

62323

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62323

Drug Name

POLYMOX

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

62323 / 2

Active Ingredient

AMOXICILLIN

Application Number

62323

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
26 Nov
Discontinued Application: 62579

Drug Name

PRECEF

Product Number

1

Dosage Form

-

Strength

500MG/VIAL

Approval Date

1984-11-26

62579 / 1

Active Ingredient

CEFORANIDE

Application Number

62579

Product Number

1

Dosage Form

-

Strength

500MG/VIAL

Approval Date

1984-11-26

Regulatory Status

Discontinued

1984
26 Nov
Discontinued Application: 62579

Drug Name

PRECEF

Product Number

2

Dosage Form

-

Strength

1GM/VIAL

Approval Date

1984-11-26

62579 / 2

Active Ingredient

CEFORANIDE

Application Number

62579

Product Number

2

Dosage Form

-

Strength

1GM/VIAL

Approval Date

1984-11-26

Regulatory Status

Discontinued

1984
26 Nov
Discontinued Application: 62579

Drug Name

PRECEF

Product Number

3

Dosage Form

-

Strength

2GM/VIAL

Approval Date

1984-11-26

62579 / 3

Active Ingredient

CEFORANIDE

Application Number

62579

Product Number

3

Dosage Form

-

Strength

2GM/VIAL

Approval Date

1984-11-26

Regulatory Status

Discontinued

1984
26 Nov
Discontinued Application: 62579

Drug Name

PRECEF

Product Number

4

Dosage Form

-

Strength

10GM/VIAL

Approval Date

1984-11-26

62579 / 4

Active Ingredient

CEFORANIDE

Application Number

62579

Product Number

4

Dosage Form

-

Strength

10GM/VIAL

Approval Date

1984-11-26

Regulatory Status

Discontinued

1984
26 Nov
Discontinued Application: 62579

Drug Name

PRECEF

Product Number

5

Dosage Form

-

Strength

20GM/VIAL

Approval Date

1984-11-26

62579 / 5

Active Ingredient

CEFORANIDE

Application Number

62579

Product Number

5

Dosage Form

-

Strength

20GM/VIAL

Approval Date

1984-11-26

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61394

Drug Name

PRINCIPEN

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/ML

Approval Date

1982-01-01

61394 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61394

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61394

Drug Name

PRINCIPEN

Product Number

2

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

61394 / 2

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61394

Product Number

2

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61394

Drug Name

PRINCIPEN

Product Number

3

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

61394 / 3

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61394

Product Number

3

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988
04 Mar
Discontinued Application: 62888

Drug Name

PRINCIPEN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1988-03-04

62888 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

62888

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1988-03-04

Regulatory Status

Discontinued

1988
04 Mar
Discontinued Application: 62888

Drug Name

PRINCIPEN

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1988-03-04

62888 / 2

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

62888

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1988-03-04

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60127

Drug Name

PRINCIPEN 125

Product Number

2

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

60127 / 2

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

60127

Product Number

2

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62151

Drug Name

PRINCIPEN 125

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

62151 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

62151

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50056

Drug Name

PRINCIPEN 250

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

50056 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

50056

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60127

Drug Name

PRINCIPEN 250

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

60127 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

60127

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62151

Drug Name

PRINCIPEN 250

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

62151 / 2

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

62151

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62157

Drug Name

PRINCIPEN 250

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

62157 / 2

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

62157

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50056

Drug Name

PRINCIPEN 500

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

50056 / 2

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

50056

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62157

Drug Name

PRINCIPEN 500

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

62157 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

62157

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50488

Drug Name

PRINCIPEN W/ PROBENECID

Product Number

1

Dosage Form

-

Strength

EQ 389MG BASE;111MG

Approval Date

1982-01-01

50488 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE; PROBENECID

Application Number

50488

Product Number

1

Dosage Form

-

Strength

EQ 389MG BASE;111MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62150

Drug Name

PRINCIPEN W/ PROBENECID

Product Number

1

Dosage Form

-

Strength

EQ 389MG BASE;111MG

Approval Date

1982-01-01

62150 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE; PROBENECID

Application Number

62150

Product Number

1

Dosage Form

-

Strength

EQ 389MG BASE;111MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11751

Drug Name

PROLIXIN

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

11751 / 1

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

11751

Product Number

1

Dosage Form

-

Strength

2.5MG **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: 11751

Drug Name

PROLIXIN

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

11751 / 2

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

11751

Product Number

2

Dosage Form

-

Strength

10MG **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: 11751

Drug Name

PROLIXIN

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1982-01-01

11751 / 3

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

11751

Product Number

3

Dosage Form

-

Strength

5MG **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: 11751

Drug Name

PROLIXIN

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-01-01

11751 / 4

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

11751

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11751

Drug Name

PROLIXIN

Product Number

5

Dosage Form

-

Strength

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

Approval Date

1982-01-01

11751 / 5

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

11751

Product Number

5

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 12145

Drug Name

PROLIXIN

Product Number

3

Dosage Form

-

Strength

2.5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

12145 / 3

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

12145

Product Number

3

Dosage Form

-

Strength

2.5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
07 Nov
Discontinued Application: 70533

Drug Name

PROLIXIN

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1985-11-07

70533 / 1

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

70533

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1985-11-07

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16110

Drug Name

PROLIXIN ENANTHATE

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

16110 / 1

Active Ingredient

FLUPHENAZINE ENANTHATE

Application Number

16110

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 7335

Drug Name

PRONESTYL

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

7335 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

7335

Product Number

1

Dosage Form

-

Strength

250MG **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: 7335

Drug Name

PRONESTYL

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

7335 / 2

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

7335

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 7335

Drug Name

PRONESTYL

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1982-01-01

7335 / 3

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

7335

Product Number

3

Dosage Form

-

Strength

500MG **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: 7335

Drug Name

PRONESTYL

Product Number

4

Dosage Form

-

Strength

375MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

7335 / 4

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

7335

Product Number

4

Dosage Form

-

Strength

375MG **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: 7335

Drug Name

PRONESTYL

Product Number

5

Dosage Form

-

Strength

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

Approval Date

1982-01-01

7335 / 5

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

7335

Product Number

5

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17371

Drug Name

PRONESTYL

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

17371 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

17371

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17371

Drug Name

PRONESTYL

Product Number

2

Dosage Form

-

Strength

375MG

Approval Date

1982-01-01

17371 / 2

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

17371

Product Number

2

Dosage Form

-

Strength

375MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17371

Drug Name

PRONESTYL

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

17371 / 3

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

17371

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87361

Drug Name

PRONESTYL-SR

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

87361 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

87361

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50118

Drug Name

PROSTAPHLIN

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

50118 / 2

Active Ingredient

OXACILLIN SODIUM

Application Number

50118

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50194

Drug Name

PROSTAPHLIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

50194 / 1

Active Ingredient

OXACILLIN SODIUM

Application Number

50194

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1994
28 Apr
Discontinued Application: 73403

Drug Name

QUESTRAN

Product Number

1

Dosage Form

-

Strength

EQ 1GM RESIN

Approval Date

1994-04-28

73403 / 1

Active Ingredient

CHOLESTYRAMINE

Application Number

73403

Product Number

1

Dosage Form

-

Strength

EQ 1GM RESIN

Approval Date

1994-04-28

Regulatory Status

Discontinued

1999
27 Dec
Discontinued Application: 73403

Drug Name

QUESTRAN

Product Number

2

Dosage Form

-

Strength

EQ 800MG RESIN

Approval Date

1999-12-27

73403 / 2

Active Ingredient

CHOLESTYRAMINE

Application Number

73403

Product Number

2

Dosage Form

-

Strength

EQ 800MG RESIN

Approval Date

1999-12-27

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 8842

Drug Name

RAUDIXIN

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

8842 / 1

Active Ingredient

RAUWOLFIA SERPENTINA ROOT

Application Number

8842

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 8842

Drug Name

RAUDIXIN

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

8842 / 2

Active Ingredient

RAUWOLFIA SERPENTINA ROOT

Application Number

8842

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17857

Drug Name

STADOL

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-01-01

17857 / 4

Active Ingredient

BUTORPHANOL TARTRATE

Application Number

17857

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17857

Drug Name

STADOL PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

17857 / 1

Active Ingredient

BUTORPHANOL TARTRATE

Application Number

17857

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17857

Drug Name

STADOL PRESERVATIVE FREE

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

17857 / 2

Active Ingredient

BUTORPHANOL TARTRATE

Application Number

17857

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50117

Drug Name

STAPHCILLIN

Product Number

1

Dosage Form

-

Strength

EQ 900MG BASE/VIAL

Approval Date

1982-01-01

50117 / 1

Active Ingredient

METHICILLIN SODIUM

Application Number

50117

Product Number

1

Dosage Form

-

Strength

EQ 900MG BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50117

Drug Name

STAPHCILLIN

Product Number

2

Dosage Form

-

Strength

EQ 3.6GM BASE/VIAL

Approval Date

1982-01-01

50117 / 2

Active Ingredient

METHICILLIN SODIUM

Application Number

50117

Product Number

2

Dosage Form

-

Strength

EQ 3.6GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50117

Drug Name

STAPHCILLIN

Product Number

3

Dosage Form

-

Strength

EQ 5.4GM BASE/VIAL

Approval Date

1982-01-01

50117 / 3

Active Ingredient

METHICILLIN SODIUM

Application Number

50117

Product Number

3

Dosage Form

-

Strength

EQ 5.4GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61449

Drug Name

STAPHCILLIN

Product Number

1

Dosage Form

-

Strength

EQ 900MG BASE/VIAL

Approval Date

1982-01-01

61449 / 1

Active Ingredient

METHICILLIN SODIUM

Application Number

61449

Product Number

1

Dosage Form

-

Strength

EQ 900MG BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61449

Drug Name

STAPHCILLIN

Product Number

2

Dosage Form

-

Strength

EQ 3.6GM BASE/VIAL

Approval Date

1982-01-01

61449 / 2

Active Ingredient

METHICILLIN SODIUM

Application Number

61449

Product Number

2

Dosage Form

-

Strength

EQ 3.6GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61449

Drug Name

STAPHCILLIN

Product Number

3

Dosage Form

-

Strength

EQ 5.4GM BASE/VIAL

Approval Date

1982-01-01

61449 / 3

Active Ingredient

METHICILLIN SODIUM

Application Number

61449

Product Number

3

Dosage Form

-

Strength

EQ 5.4GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 8847

Drug Name

SUCOSTRIN

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

1982-01-01

8847 / 1

Active Ingredient

SUCCINYLCHOLINE CHLORIDE

Application Number

8847

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 8847

Drug Name

SUCOSTRIN

Product Number

3

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

8847 / 3

Active Ingredient

SUCCINYLCHOLINE CHLORIDE

Application Number

8847

Product Number

3

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60429

Drug Name

SUMYCIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

60429 / 1

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

60429

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60429

Drug Name

SUMYCIN

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

60429 / 2

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

60429

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60429

Drug Name

SUMYCIN

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

60429 / 3

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

60429

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60429

Drug Name

SUMYCIN

Product Number

4

Dosage Form

-

Strength

125MG

Approval Date

1982-01-01

60429 / 4

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

60429

Product Number

4

Dosage Form

-

Strength

125MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50192

Drug Name

TEGOPEN

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

50192 / 1

Active Ingredient

CLOXACILLIN SODIUM

Application Number

50192

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61453

Drug Name

TEGOPEN

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

61453 / 1

Active Ingredient

CLOXACILLIN SODIUM

Application Number

61453

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1994
31 May
Discontinued Application: 64021

Drug Name

TOBRAMYCIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

1994-05-31

64021 / 1

Active Ingredient

TOBRAMYCIN SULFATE

Application Number

64021

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

1994-05-31

Regulatory Status

Discontinued

1994
31 May
Discontinued Application: 64021

Drug Name

TOBRAMYCIN SULFATE

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1994-05-31

64021 / 2

Active Ingredient

TOBRAMYCIN SULFATE

Application Number

64021

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1994-05-31

Regulatory Status

Discontinued

1994
31 May
Discontinued Application: 64026

Drug Name

TOBRAMYCIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1994-05-31

64026 / 1

Active Ingredient

TOBRAMYCIN SULFATE

Application Number

64026

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1994-05-31

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61885

Drug Name

TRIMOX

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

61885 / 1

Active Ingredient

AMOXICILLIN

Application Number

61885

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61885

Drug Name

TRIMOX

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

61885 / 2

Active Ingredient

AMOXICILLIN

Application Number

61885

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61886

Drug Name

TRIMOX

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

61886 / 1

Active Ingredient

AMOXICILLIN

Application Number

61886

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61886

Drug Name

TRIMOX

Product Number

2

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

61886 / 2

Active Ingredient

AMOXICILLIN

Application Number

61886

Product Number

2

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61886

Drug Name

TRIMOX

Product Number

3

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

61886 / 3

Active Ingredient

AMOXICILLIN

Application Number

61886

Product Number

3

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62098

Drug Name

TRIMOX

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

62098 / 1

Active Ingredient

AMOXICILLIN

Application Number

62098

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62098

Drug Name

TRIMOX

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

62098 / 2

Active Ingredient

AMOXICILLIN

Application Number

62098

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62099

Drug Name

TRIMOX

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

62099 / 1

Active Ingredient

AMOXICILLIN

Application Number

62099

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62099

Drug Name

TRIMOX

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

62099 / 2

Active Ingredient

AMOXICILLIN

Application Number

62099

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62152

Drug Name

TRIMOX

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

62152 / 1

Active Ingredient

AMOXICILLIN

Application Number

62152

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62152

Drug Name

TRIMOX

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

62152 / 2

Active Ingredient

AMOXICILLIN

Application Number

62152

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62154

Drug Name

TRIMOX

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

62154 / 1

Active Ingredient

AMOXICILLIN

Application Number

62154

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62154

Drug Name

TRIMOX

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

62154 / 2

Active Ingredient

AMOXICILLIN

Application Number

62154

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988
08 Mar
Discontinued Application: 62885

Drug Name

TRIMOX

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1988-03-08

62885 / 1

Active Ingredient

AMOXICILLIN

Application Number

62885

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1988-03-08

Regulatory Status

Discontinued

1988
08 Mar
Discontinued Application: 62885

Drug Name

TRIMOX

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1988-03-08

62885 / 2

Active Ingredient

AMOXICILLIN

Application Number

62885

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1988-03-08

Regulatory Status

Discontinued

1992
20 Mar
Discontinued Application: 63099

Drug Name

TRIMOX

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1992-03-20

63099 / 1

Active Ingredient

AMOXICILLIN

Application Number

63099

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1992-03-20

Regulatory Status

Discontinued

1992
20 Mar
Discontinued Application: 63099

Drug Name

TRIMOX

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1992-03-20

63099 / 2

Active Ingredient

AMOXICILLIN

Application Number

63099

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1992-03-20

Regulatory Status

Discontinued

1982
10 Jun
Discontinued Application: 62390

Drug Name

ULTRACEF

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

1982-06-10

62390 / 1

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

62390

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

1982-06-10

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61410

Drug Name

VEETIDS

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

61410 / 1

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61410

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61410

Drug Name

VEETIDS

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

61410 / 2

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61410

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61411

Drug Name

VEETIDS

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

61411 / 1

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61411

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61411

Drug Name

VEETIDS

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

61411 / 2

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61411

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61206

Drug Name

VEETIDS 125

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

61206 / 1

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61206

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62153

Drug Name

VEETIDS 125

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

62153 / 1

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

62153

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61164

Drug Name

VEETIDS 250

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

61164 / 1

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61164

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61206

Drug Name

VEETIDS 250

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

61206 / 2

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61206

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62153

Drug Name

VEETIDS 250

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

62153 / 2

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

62153

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62156

Drug Name

VEETIDS 250

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

62156 / 2

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

62156

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61164

Drug Name

VEETIDS 500

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

61164 / 2

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61164

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 62156

Drug Name

VEETIDS 500

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

62156 / 1

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

62156

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61764

Drug Name

VELOSEF

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

61764 / 1

Active Ingredient

CEPHRADINE

Application Number

61764

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61764

Drug Name

VELOSEF

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

61764 / 2

Active Ingredient

CEPHRADINE

Application Number

61764

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61976

Drug Name

VELOSEF

Product Number

1

Dosage Form

-

Strength

250MG/VIAL

Approval Date

1982-01-01

61976 / 1

Active Ingredient

CEPHRADINE

Application Number

61976

Product Number

1

Dosage Form

-

Strength

250MG/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61976

Drug Name

VELOSEF

Product Number

2

Dosage Form

-

Strength

500MG/VIAL

Approval Date

1982-01-01

61976 / 2

Active Ingredient

CEPHRADINE

Application Number

61976

Product Number

2

Dosage Form

-

Strength

500MG/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61976

Drug Name

VELOSEF

Product Number

3

Dosage Form

-

Strength

2GM/VIAL

Approval Date

1982-01-01

61976 / 3

Active Ingredient

CEPHRADINE

Application Number

61976

Product Number

3

Dosage Form

-

Strength

2GM/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61976

Drug Name

VELOSEF

Product Number

4

Dosage Form

-

Strength

1GM/VIAL

Approval Date

1982-01-01

61976 / 4

Active Ingredient

CEPHRADINE

Application Number

61976

Product Number

4

Dosage Form

-

Strength

1GM/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61976

Drug Name

VELOSEF

Product Number

5

Dosage Form

-

Strength

4GM/VIAL

Approval Date

1982-01-01

61976 / 5

Active Ingredient

CEPHRADINE

Application Number

61976

Product Number

5

Dosage Form

-

Strength

4GM/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61763

Drug Name

VELOSEF 125

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

61763 / 1

Active Ingredient

CEPHRADINE

Application Number

61763

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61763

Drug Name

VELOSEF 250

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

61763 / 2

Active Ingredient

CEPHRADINE

Application Number

61763

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11325

Drug Name

VESPRIN

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

1982-01-01

11325 / 1

Active Ingredient

TRIFLUPROMAZINE HYDROCHLORIDE

Application Number

11325

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11325

Drug Name

VESPRIN

Product Number

4

Dosage Form

-

Strength

10MG/ML

Approval Date

1982-01-01

11325 / 4

Active Ingredient

TRIFLUPROMAZINE HYDROCHLORIDE

Application Number

11325

Product Number

4

Dosage Form

-

Strength

10MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11325

Drug Name

VESPRIN

Product Number

5

Dosage Form

-

Strength

3MG/ML

Approval Date

1982-01-01

11325 / 5

Active Ingredient

TRIFLUPROMAZINE HYDROCHLORIDE

Application Number

11325

Product Number

5

Dosage Form

-

Strength

3MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11491

Drug Name

VESPRIN

Product Number

4

Dosage Form

-

Strength

EQ 50MG HYDROCHLORIDE/5ML

Approval Date

1982-01-01

11491 / 4

Active Ingredient

TRIFLUPROMAZINE

Application Number

11491

Product Number

4

Dosage Form

-

Strength

EQ 50MG HYDROCHLORIDE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

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  • FDA Approved Drugs Database
    246 View
Drug Status Breakdown
246 total
  • Discontinued
  • 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

ACYCLOVIR SODIUM

Application Number

74897

Product Number

1

Active Ingredient

ACYCLOVIR SODIUM

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

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Organized FDA drug records

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