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Temovate
Temovate - 0462-0269-50 - (Clobetasol Propionate)
Drug Information of Temovate
| Product NDC: | 0462-0269 |
| Proprietary Name: | Temovate |
| 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) |
Labeler Information of Temovate
| Product NDC: | 0462-0269 |
| Labeler Name: | PharmaDerm, A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019966 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19900222 |
Package Information of Temovate
| Package NDC: | 0462-0269-50 |
| Package Description: | 50 mL in 1 BOTTLE, PLASTIC (0462-0269-50) |
NDC Information of Temovate
| NDC Code | 0462-0269-50 |
| Proprietary Name | Temovate |
| Package Description | 50 mL in 1 BOTTLE, PLASTIC (0462-0269-50) |
| Product NDC | 0462-0269 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clobetasol Propionate |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19900222 |
| Marketing Category Name | NDA |
| Labeler Name | PharmaDerm, A division of Fougera Pharmaceuticals Inc. |
| Substance Name | CLOBETASOL PROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
