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Fluocinonide - 51672-1273-4 - (Fluocinonide)

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Drug Information of Fluocinonide

Product NDC: 51672-1273
Proprietary Name: Fluocinonide
Non Proprietary Name: Fluocinonide
Active Ingredient(s): .5    mg/mL & nbsp;   Fluocinonide
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fluocinonide

Product NDC: 51672-1273
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074799
Marketing Category: ANDA
Start Marketing Date: 19961231

Package Information of Fluocinonide

Package NDC: 51672-1273-4
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (51672-1273-4) > 60 mL in 1 BOTTLE, PLASTIC

NDC Information of Fluocinonide

NDC Code 51672-1273-4
Proprietary Name Fluocinonide
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (51672-1273-4) > 60 mL in 1 BOTTLE, PLASTIC
Product NDC 51672-1273
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluocinonide
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 19961231
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name FLUOCINONIDE
Strength Number .5
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Fluocinonide


General Information