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Clobetasol Propionate
Clobetasol Propionate - 50436-9985-1 - (clobetasol propionate)
Drug Information of Clobetasol Propionate
| Product NDC: | 50436-9985 |
| 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): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clobetasol Propionate
| Product NDC: | 50436-9985 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074392 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960930 |
Package Information of Clobetasol Propionate
| Package NDC: | 50436-9985-1 |
| Package Description: | 45 g in 1 TUBE (50436-9985-1) |
NDC Information of Clobetasol Propionate
| NDC Code | 50436-9985-1 |
| Proprietary Name | Clobetasol Propionate |
| Package Description | 45 g in 1 TUBE (50436-9985-1) |
| Product NDC | 50436-9985 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clobetasol propionate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19960930 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | CLOBETASOL PROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
