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Clobetasol Propionate - 51672-1259-1 - (Clobetasol Propionate)

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Drug Information of Clobetasol Propionate

Product NDC: 51672-1259
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: 51672-1259
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074248
Marketing Category: ANDA
Start Marketing Date: 19960712

Package Information of Clobetasol Propionate

Package NDC: 51672-1259-1
Package Description: 1 TUBE in 1 CARTON (51672-1259-1) > 15 g in 1 TUBE

NDC Information of Clobetasol Propionate

NDC Code 51672-1259-1
Proprietary Name Clobetasol Propionate
Package Description 1 TUBE in 1 CARTON (51672-1259-1) > 15 g in 1 TUBE
Product NDC 51672-1259
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clobetasol Propionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19960712
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., 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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