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Halobetasol Propionate - 54868-5482-0 - (halobetasol propionate)

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Drug Information of Halobetasol Propionate

Product NDC: 54868-5482
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: 54868-5482
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076872
Marketing Category: ANDA
Start Marketing Date: 20051205

Package Information of Halobetasol Propionate

Package NDC: 54868-5482-0
Package Description: 1 TUBE in 1 CARTON (54868-5482-0) > 15 g in 1 TUBE

NDC Information of Halobetasol Propionate

NDC Code 54868-5482-0
Proprietary Name Halobetasol Propionate
Package Description 1 TUBE in 1 CARTON (54868-5482-0) > 15 g in 1 TUBE
Product NDC 54868-5482
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name halobetasol propionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20051205
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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