TEMOVATE E - 10337-301-60 - (clobetasol propionate)

Alphabetical Index


Drug Information of TEMOVATE E

Product NDC: 10337-301
Proprietary Name: TEMOVATE E
Non Proprietary Name: clobetasol propionate
Active Ingredient(s): .5    mg/g & nbsp;   clobetasol propionate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of TEMOVATE E

Product NDC: 10337-301
Labeler Name: PharmaDerm a division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020340
Marketing Category: NDA
Start Marketing Date: 19940617

Package Information of TEMOVATE E

Package NDC: 10337-301-60
Package Description: 1 TUBE in 1 CARTON (10337-301-60) > 60 g in 1 TUBE

NDC Information of TEMOVATE E

NDC Code 10337-301-60
Proprietary Name TEMOVATE E
Package Description 1 TUBE in 1 CARTON (10337-301-60) > 60 g in 1 TUBE
Product NDC 10337-301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clobetasol propionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19940617
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 E


General Information