Product NDC: | 51672-1350 |
Proprietary Name: | Clobetasol Propionate |
Non Proprietary Name: | clobetasol propionate |
Active Ingredient(s): | .5 mg/mL & nbsp; clobetasol propionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51672-1350 |
Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA200302 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120702 |
Package NDC: | 51672-1350-4 |
Package Description: | 1 BOTTLE in 1 CARTON (51672-1350-4) > 59 mL in 1 BOTTLE |
NDC Code | 51672-1350-4 |
Proprietary Name | Clobetasol Propionate |
Package Description | 1 BOTTLE in 1 CARTON (51672-1350-4) > 59 mL in 1 BOTTLE |
Product NDC | 51672-1350 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clobetasol propionate |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120702 |
Marketing Category Name | ANDA |
Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
Substance Name | CLOBETASOL PROPIONATE |
Strength Number | .5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |