Product NDC: | 0095-0049 |
Proprietary Name: | Cormax |
Non Proprietary Name: | Clobetasol Propionate |
Active Ingredient(s): | .4625 mg/mL & nbsp; Clobetasol Propionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0095-0049 |
Labeler Name: | ECR Pharmaceuticals Co., Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074222 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120705 |
Package NDC: | 0095-0049-50 |
Package Description: | 1 BOTTLE in 1 CARTON (0095-0049-50) > 50 mL in 1 BOTTLE |
NDC Code | 0095-0049-50 |
Proprietary Name | Cormax |
Package Description | 1 BOTTLE in 1 CARTON (0095-0049-50) > 50 mL in 1 BOTTLE |
Product NDC | 0095-0049 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clobetasol Propionate |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20120705 |
Marketing Category Name | ANDA |
Labeler Name | ECR Pharmaceuticals Co., Inc. |
Substance Name | CLOBETASOL PROPIONATE |
Strength Number | .4625 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |