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Fluocinonide - 21695-207-30 - (Fluocinonide)

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Drug Information of Fluocinonide

Product NDC: 21695-207
Proprietary Name: Fluocinonide
Non Proprietary Name: Fluocinonide
Active Ingredient(s): .5    mg/g & nbsp;   Fluocinonide
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Fluocinonide

Product NDC: 21695-207
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA019117
Marketing Category: ANDA
Start Marketing Date: 19840626

Package Information of Fluocinonide

Package NDC: 21695-207-30
Package Description: 1 TUBE in 1 CARTON (21695-207-30) > 30 g in 1 TUBE

NDC Information of Fluocinonide

NDC Code 21695-207-30
Proprietary Name Fluocinonide
Package Description 1 TUBE in 1 CARTON (21695-207-30) > 30 g in 1 TUBE
Product NDC 21695-207
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluocinonide
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19840626
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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