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CLOBETASOL PROPIONATE - 54868-6291-0 - (clobetasol propionate)

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Drug Information of CLOBETASOL PROPIONATE

Product NDC: 54868-6291
Proprietary Name: CLOBETASOL PROPIONATE
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 CLOBETASOL PROPIONATE

Product NDC: 54868-6291
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021142
Marketing Category: NDA
Start Marketing Date: 20110816

Package Information of CLOBETASOL PROPIONATE

Package NDC: 54868-6291-0
Package Description: 50 g in 1 CAN (54868-6291-0)

NDC Information of CLOBETASOL PROPIONATE

NDC Code 54868-6291-0
Proprietary Name CLOBETASOL PROPIONATE
Package Description 50 g in 1 CAN (54868-6291-0)
Product NDC 54868-6291
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clobetasol propionate
Dosage Form Name AEROSOL, FOAM
Route Name TOPICAL
Start Marketing Date 20110816
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 CLOBETASOL PROPIONATE


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