Product NDC: | 21695-358 |
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): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-358 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075205 |
Marketing Category: | ANDA |
Start Marketing Date: | 19981113 |
Package NDC: | 21695-358-25 |
Package Description: | 25 mL in 1 BOTTLE (21695-358-25) |
NDC Code | 21695-358-25 |
Proprietary Name | Clobetasol Propionate |
Package Description | 25 mL in 1 BOTTLE (21695-358-25) |
Product NDC | 21695-358 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clobetasol Propionate |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19981113 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | CLOBETASOL PROPIONATE |
Strength Number | .5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |