Pierre Fabre
FDA Approved Drugs

Pierre Fabre

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 2
  • Latest Approval Date Jul 09, 1997
  • Data Source FDA
  • First Approval Date Dec 23, 1994
Company Overview

Company

Pierre Fabre

Country

France

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Company Snapshot

Pierre Fabre

3, Avenue Hubert Curien Toulouse, Occitanie 31100

France

www.pierre-fabre.com/fr enquiries@pharmacompass.com View on Map
FDA Approved Drug Records ( 2 records )
1997
09 Jul
Discontinued Application: 74813

Drug Name

ETOPOSIDE

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

1997-07-09

74813 / 1

Active Ingredient

ETOPOSIDE

Application Number

74813

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

1997-07-09

Regulatory Status

Discontinued

1994
23 Dec
Discontinued Application: 20388

Drug Name

NAVELBINE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-23

20388 / 1

Active Ingredient

VINORELBINE TARTRATE

Application Number

20388

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-23

Regulatory Status

Discontinued

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Drug Status Breakdown
2 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

ETOPOSIDE

Application Number

74813

Product Number

1

Active Ingredient

ETOPOSIDE

Dosage Form

-

Strength

20MG/ML

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