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Halobetasol Propionate - 0168-0355-50 - (halobetasol propionate)

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Drug Information of Halobetasol Propionate

Product NDC: 0168-0355
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: 0168-0355
Labeler Name: E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077001
Marketing Category: ANDA
Start Marketing Date: 20041216

Package Information of Halobetasol Propionate

Package NDC: 0168-0355-50
Package Description: 50 g in 1 TUBE (0168-0355-50)

NDC Information of Halobetasol Propionate

NDC Code 0168-0355-50
Proprietary Name Halobetasol Propionate
Package Description 50 g in 1 TUBE (0168-0355-50)
Product NDC 0168-0355
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name halobetasol propionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20041216
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO., A division of Fougera Pharmaceuticals 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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