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Fluocinonide - 21695-979-30 - (Fluocinonide)

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Drug Information of Fluocinonide

Product NDC: 21695-979
Proprietary Name: Fluocinonide
Non Proprietary Name: Fluocinonide
Active Ingredient(s): .5    mg/g & nbsp;   Fluocinonide
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Fluocinonide

Product NDC: 21695-979
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073481
Marketing Category: ANDA
Start Marketing Date: 20110120

Package Information of Fluocinonide

Package NDC: 21695-979-30
Package Description: 30 g in 1 TUBE (21695-979-30)

NDC Information of Fluocinonide

NDC Code 21695-979-30
Proprietary Name Fluocinonide
Package Description 30 g in 1 TUBE (21695-979-30)
Product NDC 21695-979
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluocinonide
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20110120
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


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