Johnson & Johnson
FDA Approved Drugs

Johnson & Johnson

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

Discontinued
  • Total Records 6
  • Latest Approval Date Dec 28, 1990
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

Johnson & Johnson

Country

U.S.A

Website

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Email

eknewitz@its.jnj.com

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Company Snapshot

Johnson & Johnson

One Johnson & Johnson PlazaNew Brunswick, New Jersey 08933

U.S.A

www.jnj.com/ eknewitz@its.jnj.com View on Map
FDA Approved Drug Records ( 6 records )
1985
15 Feb
Discontinued Application: 50594

Drug Name

ERYCETTE

Product Number

1

Dosage Form

-

Strength

2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-02-15

50594 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

50594

Product Number

1

Dosage Form

-

Strength

2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-02-15

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50448

Drug Name

GRIFULVIN V

Product Number

1

Dosage Form

-

Strength

125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50448 / 1

Active Ingredient

GRISEOFULVIN, MICROCRYSTALLINE

Application Number

50448

Product Number

1

Dosage Form

-

Strength

125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 50518

Drug Name

MECLAN

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

50518 / 1

Active Ingredient

MECLOCYCLINE SULFOSALICYLATE

Application Number

50518

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1990
28 Dec
Discontinued Application: 19002

Drug Name

VASCOR

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1990-12-28

19002 / 1

Active Ingredient

BEPRIDIL HYDROCHLORIDE

Application Number

19002

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1990-12-28

Regulatory Status

Discontinued

1990
28 Dec
Discontinued Application: 19002

Drug Name

VASCOR

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

1990-12-28

19002 / 2

Active Ingredient

BEPRIDIL HYDROCHLORIDE

Application Number

19002

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

1990-12-28

Regulatory Status

Discontinued

1990
28 Dec
Discontinued Application: 19002

Drug Name

VASCOR

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

1990-12-28

19002 / 3

Active Ingredient

BEPRIDIL HYDROCHLORIDE

Application Number

19002

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

1990-12-28

Regulatory Status

Discontinued

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Drug Status Breakdown
6 total
  • Discontinued
Official Source

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

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FDA Approved Drug Record Details Preview

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

Drug Name

ERYCETTE

Application Number

50594

Product Number

1

Active Ingredient

ERYTHROMYCIN

Dosage Form

-

Strength

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

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