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Halobetasol Propionate - 51672-1322-5 - (Halobetasol Propionate)

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Drug Information of Halobetasol Propionate

Product NDC: 51672-1322
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): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Halobetasol Propionate

Product NDC: 51672-1322
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076994
Marketing Category: ANDA
Start Marketing Date: 20041216

Package Information of Halobetasol Propionate

Package NDC: 51672-1322-5
Package Description: 5 g in 1 TUBE (51672-1322-5)

NDC Information of Halobetasol Propionate

NDC Code 51672-1322-5
Proprietary Name Halobetasol Propionate
Package Description 5 g in 1 TUBE (51672-1322-5)
Product NDC 51672-1322
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Halobetasol Propionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20041216
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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