Home > National Drug Code (NDC) > Clobetasol Propionate

Clobetasol Propionate - 21695-358-25 - (Clobetasol Propionate)

Alphabetical Index


Drug Information of Clobetasol Propionate

Product NDC: 21695-358
Proprietary Name: Clobetasol Propionate
Non Proprietary Name: Clobetasol Propionate
Active Ingredient(s): .5    mg/mL & nbsp;   Clobetasol Propionate
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Clobetasol Propionate

Product NDC: 21695-358
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075205
Marketing Category: ANDA
Start Marketing Date: 19981113

Package Information of Clobetasol Propionate

Package NDC: 21695-358-25
Package Description: 25 mL in 1 BOTTLE (21695-358-25)

NDC Information of Clobetasol Propionate

NDC Code 21695-358-25
Proprietary Name Clobetasol Propionate
Package Description 25 mL in 1 BOTTLE (21695-358-25)
Product NDC 21695-358
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clobetasol Propionate
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 19981113
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name CLOBETASOL PROPIONATE
Strength Number .5
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Clobetasol Propionate


General Information