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Fluocinolone Acetonide - 0713-0222-60 - (Fluocinolone Acetonide)

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Drug Information of Fluocinolone Acetonide

Product NDC: 0713-0222
Proprietary Name: Fluocinolone Acetonide
Non Proprietary Name: Fluocinolone Acetonide
Active Ingredient(s): .25    mg/g & nbsp;   Fluocinolone Acetonide
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Fluocinolone Acetonide

Product NDC: 0713-0222
Labeler Name: GW Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089525
Marketing Category: ANDA
Start Marketing Date: 19880726

Package Information of Fluocinolone Acetonide

Package NDC: 0713-0222-60
Package Description: 60 g in 1 TUBE (0713-0222-60)

NDC Information of Fluocinolone Acetonide

NDC Code 0713-0222-60
Proprietary Name Fluocinolone Acetonide
Package Description 60 g in 1 TUBE (0713-0222-60)
Product NDC 0713-0222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluocinolone Acetonide
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19880726
Marketing Category Name ANDA
Labeler Name GW Laboratories, Inc.
Substance Name FLUOCINOLONE ACETONIDE
Strength Number .25
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Fluocinolone Acetonide


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