| 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] |