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: | 0472-0404-91 |
Package Description: | 1 BOTTLE in 1 CARTON (0472-0404-91) > 30 mL in 1 BOTTLE |
NDC Code | 0472-0404-91 |
Proprietary Name | Clobetasol Propionate |
Package Description | 1 BOTTLE in 1 CARTON (0472-0404-91) > 30 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] |