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Halobetasol Propionate - 51672-1321-3 - (Halobetasol Propionate)

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Drug Information of Halobetasol Propionate

Product NDC: 51672-1321
Proprietary Name: Halobetasol Propionate
Non Proprietary Name: Halobetasol Propionate
Active Ingredient(s): .5    mg/g & nbsp;   Halobetasol Propionate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Halobetasol Propionate

Product NDC: 51672-1321
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077227
Marketing Category: ANDA
Start Marketing Date: 20050804

Package Information of Halobetasol Propionate

Package NDC: 51672-1321-3
Package Description: 1 TUBE in 1 CARTON (51672-1321-3) > 50 g in 1 TUBE

NDC Information of Halobetasol Propionate

NDC Code 51672-1321-3
Proprietary Name Halobetasol Propionate
Package Description 1 TUBE in 1 CARTON (51672-1321-3) > 50 g in 1 TUBE
Product NDC 51672-1321
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Halobetasol Propionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20050804
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name HALOBETASOL PROPIONATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Halobetasol Propionate


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