Product NDC: | 0781-7137 |
Proprietary Name: | clobetasol propionate |
Non Proprietary Name: | clobetasol propionate |
Active Ingredient(s): | .05 g/100mL & nbsp; clobetasol propionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SHAMPOO |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0781-7137 |
Labeler Name: | Sandoz Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021644 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20111222 |
Package NDC: | 0781-7137-04 |
Package Description: | 1 BOTTLE in 1 CARTON (0781-7137-04) > 118 mL in 1 BOTTLE |
NDC Code | 0781-7137-04 |
Proprietary Name | clobetasol propionate |
Package Description | 1 BOTTLE in 1 CARTON (0781-7137-04) > 118 mL in 1 BOTTLE |
Product NDC | 0781-7137 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clobetasol propionate |
Dosage Form Name | SHAMPOO |
Route Name | TOPICAL |
Start Marketing Date | 20111222 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Sandoz Inc. |
Substance Name | CLOBETASOL PROPIONATE |
Strength Number | .05 |
Strength Unit | g/100mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |