Biofrontera Discontinued
FDA Approved Drugs

Biofrontera Discontinued

FDA Approved Drugs Database

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

Discontinued
  • Total Records 1
  • Latest Approval Date Nov 27, 2000
  • Data Source FDA
  • First Approval Date Nov 27, 2000
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Discontinued
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Company Overview

Company

Biofrontera Discontinued

Country

U.S.A

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Company Snapshot

Biofrontera Discontinued

201 Edgewater Dr Ste 210 Wakefield, MA 01880

U.S.A

www.biofrontera-us.com/ info-us@biofrontera.com View on Map
FDA Approved Drug Records ( 1 record )
2000
27 Nov
Discontinued Application: 50769

Drug Name

AKTIPAK

Product Number

1

Dosage Form

-

Strength

5%;3%

Approval Date

2000-11-27

50769 / 1

Active Ingredient

BENZOYL PEROXIDE; ERYTHROMYCIN

Application Number

50769

Product Number

1

Dosage Form

-

Strength

5%;3%

Approval Date

2000-11-27

Regulatory Status

Discontinued

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Drug Status Breakdown
1 total
  • Discontinued
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Explore important FDA approved drug information available in the records above.

Drug Name

AKTIPAK

Application Number

50769

Product Number

1

Active Ingredient

BENZOYL PEROXIDE; ERYTHROMYCIN

Dosage Form

-

Strength

5%;3%

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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