| 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] |