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Clobetasol Propionate - 0168-0162-30 - (clobetasol propionate)

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Drug Information of Clobetasol Propionate

Product NDC: 0168-0162
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): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Clobetasol Propionate

Product NDC: 0168-0162
Labeler Name: E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074407
Marketing Category: ANDA
Start Marketing Date: 19960223

Package Information of Clobetasol Propionate

Package NDC: 0168-0162-30
Package Description: 30 g in 1 TUBE (0168-0162-30)

NDC Information of Clobetasol Propionate

NDC Code 0168-0162-30
Proprietary Name Clobetasol Propionate
Package Description 30 g in 1 TUBE (0168-0162-30)
Product NDC 0168-0162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clobetasol propionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19960223
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO., A division of Fougera Pharmaceuticals 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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