Biofrontera
FDA Approved Drugs

Biofrontera

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 2
  • Latest Approval Date May 10, 2016
  • Data Source FDA
  • First Approval Date Nov 27, 2000
All
2
View
Discontinued
1
View
RX
1
View
Company Overview

Company

Biofrontera

Country

U.S.A

Social Profiles

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Company Snapshot

Biofrontera

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 ( 2 records )
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

2016
10 May
RX Application: 208081

Drug Name

AMELUZ

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

2016-05-10

208081 / 1

Active Ingredient

AMINOLEVULINIC ACID HYDROCHLORIDE

Application Number

208081

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

2016-05-10

Regulatory Status

RX

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Drug Status Breakdown
2 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

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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