| Product NDC: | 0472-0404 |
| 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): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0472-0404 |
| Labeler Name: | Actavis Mid Atlantic LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078223 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120103 |
| Package NDC: | 0472-0404-94 |
| Package Description: | 1 BOTTLE in 1 CARTON (0472-0404-94) > 118 mL in 1 BOTTLE |
| NDC Code | 0472-0404-94 |
| Proprietary Name | Clobetasol Propionate |
| Package Description | 1 BOTTLE in 1 CARTON (0472-0404-94) > 118 mL in 1 BOTTLE |
| Product NDC | 0472-0404 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clobetasol Propionate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120103 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis Mid Atlantic LLC |
| Substance Name | CLOBETASOL PROPIONATE |
| Strength Number | .05 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |