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Clobetasol Propionate - 51672-1350-8 - (clobetasol propionate)

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Drug Information of Clobetasol Propionate

Product NDC: 51672-1350
Proprietary Name: Clobetasol Propionate
Non Proprietary Name: clobetasol propionate
Active Ingredient(s): .5    mg/mL & nbsp;   clobetasol propionate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Clobetasol Propionate

Product NDC: 51672-1350
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200302
Marketing Category: ANDA
Start Marketing Date: 20120702

Package Information of Clobetasol Propionate

Package NDC: 51672-1350-8
Package Description: 1 BOTTLE in 1 CARTON (51672-1350-8) > 118 mL in 1 BOTTLE

NDC Information of Clobetasol Propionate

NDC Code 51672-1350-8
Proprietary Name Clobetasol Propionate
Package Description 1 BOTTLE in 1 CARTON (51672-1350-8) > 118 mL in 1 BOTTLE
Product NDC 51672-1350
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clobetasol propionate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120702
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name CLOBETASOL PROPIONATE
Strength Number .5
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Clobetasol Propionate


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