GALDERMA LABS LP Discontinued
FDA Approved Drugs

GALDERMA LABS LP 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 9
  • Latest Approval Date Mar 17, 2010
  • Data Source FDA
  • First Approval Date Jun 15, 1988
All
30
View
Unclassified
5
View
Discontinued
9
View
OTC
2
View
RX
14
View
Company Overview

Company

GALDERMA LABS LP Discontinued

Country

U.S.A

Website

Visit Website

Email

virginie.naigeon@galderma.com

Social Profiles

Company Snapshot

GALDERMA LABS LP Discontinued

14501 N. Freeway Ft. Worth, TX 76177

U.S.A

www.galderma.com/us/ virginie.naigeon@galderma.com View on Map
FDA Approved Drug Records ( 9 records )
1990
27 Aug
Discontinued Application: 20001

Drug Name

CAPEX

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1990-08-27

20001 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

20001

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1990-08-27

Regulatory Status

Discontinued

1988
15 Jun
Discontinued Application: 71425

Drug Name

DESOWEN

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

1988-06-15

71425 / 1

Active Ingredient

DESONIDE

Application Number

71425

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

1988-06-15

Regulatory Status

Discontinued

1992
24 Jan
Discontinued Application: 72354

Drug Name

DESOWEN

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

1992-01-24

72354 / 1

Active Ingredient

DESONIDE

Application Number

72354

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

1992-01-24

Regulatory Status

Discontinued

1996
31 May
Discontinued Application: 20338

Drug Name

DIFFERIN

Product Number

1

Dosage Form

-

Strength

0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-05-31

20338 / 1

Active Ingredient

ADAPALENE

Application Number

20338

Product Number

1

Dosage Form

-

Strength

0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-05-31

Regulatory Status

Discontinued

2010
17 Mar
Discontinued Application: 22502

Drug Name

DIFFERIN

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2010-03-17

22502 / 1

Active Ingredient

ADAPALENE

Application Number

22502

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2010-03-17

Regulatory Status

Discontinued

2008
08 Dec
Discontinued Application: 22320

Drug Name

EPIDUO

Product Number

1

Dosage Form

-

Strength

0.1%;2.5%

Approval Date

2008-12-08

22320 / 1

Active Ingredient

ADAPALENE; BENZOYL PEROXIDE

Application Number

22320

Product Number

1

Dosage Form

-

Strength

0.1%;2.5%

Approval Date

2008-12-08

Regulatory Status

Discontinued

1988
22 Nov
Discontinued Application: 19737

Drug Name

METROGEL

Product Number

1

Dosage Form

-

Strength

0.75% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-11-22

19737 / 1

Active Ingredient

METRONIDAZOLE

Application Number

19737

Product Number

1

Dosage Form

-

Strength

0.75% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-11-22

Regulatory Status

Discontinued

2004
27 Jul
Discontinued Application: 21415

Drug Name

METVIXIA

Product Number

1

Dosage Form

-

Strength

EQ 16.8% BASE

Approval Date

2004-07-27

21415 / 1

Active Ingredient

METHYL AMINOLEVULINATE HYDROCHLORIDE

Application Number

21415

Product Number

1

Dosage Form

-

Strength

EQ 16.8% BASE

Approval Date

2004-07-27

Regulatory Status

Discontinued

2001
02 Feb
Discontinued Application: 50783

Drug Name

PERIOSTAT

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2001-02-02

50783 / 1

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

50783

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2001-02-02

Regulatory Status

Discontinued

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Drug Status Breakdown
9 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

CAPEX

Application Number

20001

Product Number

1

Active Ingredient

FLUOCINOLONE ACETONIDE

Dosage Form

-

Strength

0.01%

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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