Home > National Drug Code (NDC) > Halobetasol Propionate

Halobetasol Propionate - 0713-0640-86 - (Halobetasol Propionate)

Alphabetical Index


Drug Information of Halobetasol Propionate

Product NDC: 0713-0640
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: 0713-0640
Labeler Name: GW Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078162
Marketing Category: ANDA
Start Marketing Date: 20070716

Package Information of Halobetasol Propionate

Package NDC: 0713-0640-86
Package Description: 50 g in 1 TUBE (0713-0640-86)

NDC Information of Halobetasol Propionate

NDC Code 0713-0640-86
Proprietary Name Halobetasol Propionate
Package Description 50 g in 1 TUBE (0713-0640-86)
Product NDC 0713-0640
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Halobetasol Propionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20070716
Marketing Category Name ANDA
Labeler Name GW Laboratories, 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


General Information