Home > National Drug Code (NDC) > Fluocinolone Acetonide

Fluocinolone Acetonide - 52565-020-15 - (Fluocinolone Acetonide)

Alphabetical Index


Drug Information of Fluocinolone Acetonide

Product NDC: 52565-020
Proprietary Name: Fluocinolone Acetonide
Non Proprietary Name: Fluocinolone Acetonide
Active Ingredient(s): .25    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: 52565-020
Labeler Name: IGI Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA012787
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20121228

Package Information of Fluocinolone Acetonide

Package NDC: 52565-020-15
Package Description: 1 TUBE in 1 CARTON (52565-020-15) > 15 g in 1 TUBE

NDC Information of Fluocinolone Acetonide

NDC Code 52565-020-15
Proprietary Name Fluocinolone Acetonide
Package Description 1 TUBE in 1 CARTON (52565-020-15) > 15 g in 1 TUBE
Product NDC 52565-020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluocinolone Acetonide
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20121228
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name IGI Labs, Inc.
Substance Name FLUOCINOLONE ACETONIDE
Strength Number .25
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Fluocinolone Acetonide


General Information