Product NDC: | 21695-483 |
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): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-483 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074407 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960223 |
Package NDC: | 21695-483-30 |
Package Description: | 30 g in 1 TUBE (21695-483-30) |
NDC Code | 21695-483-30 |
Proprietary Name | clobetasol propionate |
Package Description | 30 g in 1 TUBE (21695-483-30) |
Product NDC | 21695-483 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clobetasol propionate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 19960223 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | CLOBETASOL PROPIONATE |
Strength Number | .5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |