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Clobetasol Propionate - 50436-9985-1 - (clobetasol propionate)

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Drug Information of Clobetasol Propionate

Product NDC: 50436-9985
Proprietary Name: Clobetasol Propionate
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 Clobetasol Propionate

Product NDC: 50436-9985
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074392
Marketing Category: ANDA
Start Marketing Date: 19960930

Package Information of Clobetasol Propionate

Package NDC: 50436-9985-1
Package Description: 45 g in 1 TUBE (50436-9985-1)

NDC Information of Clobetasol Propionate

NDC Code 50436-9985-1
Proprietary Name Clobetasol Propionate
Package Description 45 g in 1 TUBE (50436-9985-1)
Product NDC 50436-9985
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clobetasol propionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19960930
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name CLOBETASOL PROPIONATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Clobetasol Propionate


General Information