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Fluocinonide - 0168-0135-60 - (fluocinonide)

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Drug Information of Fluocinonide

Product NDC: 0168-0135
Proprietary Name: Fluocinonide
Non Proprietary Name: fluocinonide
Active Ingredient(s): .5    mg/g & nbsp;   fluocinonide
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Fluocinonide

Product NDC: 0168-0135
Labeler Name: E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072933
Marketing Category: ANDA
Start Marketing Date: 19941230

Package Information of Fluocinonide

Package NDC: 0168-0135-60
Package Description: 60 g in 1 TUBE (0168-0135-60)

NDC Information of Fluocinonide

NDC Code 0168-0135-60
Proprietary Name Fluocinonide
Package Description 60 g in 1 TUBE (0168-0135-60)
Product NDC 0168-0135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluocinonide
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 19941230
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Substance Name FLUOCINONIDE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Fluocinonide


General Information