Temovate - 10337-162-15 - (clobetasol propionate)

Alphabetical Index


Drug Information of Temovate

Product NDC: 10337-162
Proprietary Name: Temovate
Non Proprietary Name: clobetasol propionate
Active Ingredient(s): .5    mg/g & nbsp;   clobetasol propionate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Temovate

Product NDC: 10337-162
Labeler Name: PharmaDerm, A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019323
Marketing Category: NDA
Start Marketing Date: 19851227

Package Information of Temovate

Package NDC: 10337-162-15
Package Description: 1 TUBE in 1 CARTON (10337-162-15) > 15 g in 1 TUBE

NDC Information of Temovate

NDC Code 10337-162-15
Proprietary Name Temovate
Package Description 1 TUBE in 1 CARTON (10337-162-15) > 15 g in 1 TUBE
Product NDC 10337-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clobetasol propionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19851227
Marketing Category Name NDA
Labeler Name PharmaDerm, A division of Fougera Pharmaceuticals Inc.
Substance Name CLOBETASOL PROPIONATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Temovate


General Information