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Fluocinolone Acetonide - 54868-6347-0 - (Fluocinolone Acetonide)

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Drug Information of Fluocinolone Acetonide

Product NDC: 54868-6347
Proprietary Name: Fluocinolone Acetonide
Non Proprietary Name: Fluocinolone Acetonide
Active Ingredient(s): .11    mg/118.28mL & nbsp;   Fluocinolone Acetonide
Administration Route(s): TOPICAL
Dosage Form(s): OIL
Coding System: National Drug Codes(NDC)

Labeler Information of Fluocinolone Acetonide

Product NDC: 54868-6347
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201759
Marketing Category: ANDA
Start Marketing Date: 20120426

Package Information of Fluocinolone Acetonide

Package NDC: 54868-6347-0
Package Description: 1 BOTTLE in 1 CARTON (54868-6347-0) > 118.28 mL in 1 BOTTLE

NDC Information of Fluocinolone Acetonide

NDC Code 54868-6347-0
Proprietary Name Fluocinolone Acetonide
Package Description 1 BOTTLE in 1 CARTON (54868-6347-0) > 118.28 mL in 1 BOTTLE
Product NDC 54868-6347
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluocinolone Acetonide
Dosage Form Name OIL
Route Name TOPICAL
Start Marketing Date 20120426
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name FLUOCINOLONE ACETONIDE
Strength Number .11
Strength Unit mg/118.28mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Fluocinolone Acetonide


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