Product NDC: | 63094-3110 |
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): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63094-3110 |
Labeler Name: | DPT Laboratories, Ltd. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021142 |
Marketing Category: | NDA |
Start Marketing Date: | 20080312 |
Package NDC: | 63094-3110-5 |
Package Description: | 1 CAN in 1 CARTON (63094-3110-5) > 50 g in 1 CAN |
NDC Code | 63094-3110-5 |
Proprietary Name | Clobetasol Propionate |
Package Description | 1 CAN in 1 CARTON (63094-3110-5) > 50 g in 1 CAN |
Product NDC | 63094-3110 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clobetasol Propionate |
Dosage Form Name | AEROSOL, FOAM |
Route Name | TOPICAL |
Start Marketing Date | 20080312 |
Marketing Category Name | NDA |
Labeler Name | DPT Laboratories, Ltd. |
Substance Name | CLOBETASOL PROPIONATE |
Strength Number | .5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |