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Fluocinolone Acetonide - 54569-1544-0 - (fluocinolone acetonide)

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Drug Information of Fluocinolone Acetonide

Product NDC: 54569-1544
Proprietary Name: Fluocinolone Acetonide
Non Proprietary Name: fluocinolone acetonide
Active Ingredient(s): .1    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: 54569-1544
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088170
Marketing Category: ANDA
Start Marketing Date: 19821216

Package Information of Fluocinolone Acetonide

Package NDC: 54569-1544-0
Package Description: 15 g in 1 TUBE (54569-1544-0)

NDC Information of Fluocinolone Acetonide

NDC Code 54569-1544-0
Proprietary Name Fluocinolone Acetonide
Package Description 15 g in 1 TUBE (54569-1544-0)
Product NDC 54569-1544
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluocinolone acetonide
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19821216
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name FLUOCINOLONE ACETONIDE
Strength Number .1
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Fluocinolone Acetonide


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