OLUX - 54868-5421-0 - (clobetasol propionate)

Alphabetical Index


Drug Information of OLUX

Product NDC: 54868-5421
Proprietary Name: OLUX
Non Proprietary Name: clobetasol propionate
Active Ingredient(s): .5    mg/g & nbsp;   clobetasol propionate
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, FOAM
Coding System: National Drug Codes(NDC)

Labeler Information of OLUX

Product NDC: 54868-5421
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021142
Marketing Category: NDA
Start Marketing Date: 20050915

Package Information of OLUX

Package NDC: 54868-5421-0
Package Description: 50 g in 1 CAN (54868-5421-0)

NDC Information of OLUX

NDC Code 54868-5421-0
Proprietary Name OLUX
Package Description 50 g in 1 CAN (54868-5421-0)
Product NDC 54868-5421
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clobetasol propionate
Dosage Form Name AEROSOL, FOAM
Route Name TOPICAL
Start Marketing Date 20050915
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name CLOBETASOL PROPIONATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of OLUX


General Information