Product NDC: | 68788-0332 |
Proprietary Name: | Clobetasol Propionate |
Non Proprietary Name: | Clobetasol Propionate |
Active Ingredient(s): | .5 mg/g & nbsp; Clobetasol Propionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-0332 |
Labeler Name: | Preferred Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074221 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130419 |
Package NDC: | 68788-0332-3 |
Package Description: | 1 TUBE in 1 CARTON (68788-0332-3) > 30 g in 1 TUBE |
NDC Code | 68788-0332-3 |
Proprietary Name | Clobetasol Propionate |
Package Description | 1 TUBE in 1 CARTON (68788-0332-3) > 30 g in 1 TUBE |
Product NDC | 68788-0332 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clobetasol Propionate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20130419 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc. |
Substance Name | CLOBETASOL PROPIONATE |
Strength Number | .5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |