Product NDC: | 0299-3848 |
Proprietary Name: | Clobex |
Non Proprietary Name: | Clobetasol Propionate |
Active Ingredient(s): | .05 g/100mL & nbsp; Clobetasol Propionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0299-3848 |
Labeler Name: | Galderma Laboratories, L.P. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021535 |
Marketing Category: | NDA |
Start Marketing Date: | 20030801 |
Package NDC: | 0299-3848-02 |
Package Description: | 59 mL in 1 BOTTLE (0299-3848-02) |
NDC Code | 0299-3848-02 |
Proprietary Name | Clobex |
Package Description | 59 mL in 1 BOTTLE (0299-3848-02) |
Product NDC | 0299-3848 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clobetasol Propionate |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20030801 |
Marketing Category Name | NDA |
Labeler Name | Galderma Laboratories, L.P. |
Substance Name | CLOBETASOL PROPIONATE |
Strength Number | .05 |
Strength Unit | g/100mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |