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Temovate
Temovate - 0462-0163-30 - (clobetasol propionate)
Drug Information of Temovate
| Product NDC: | 0462-0163 |
| Proprietary Name: | Temovate |
| 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 Temovate
| Product NDC: | 0462-0163 |
| Labeler Name: | PharmaDerm A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019322 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19851227 |
Package Information of Temovate
| Package NDC: | 0462-0163-30 |
| Package Description: | 1 TUBE in 1 CARTON (0462-0163-30) > 30 g in 1 TUBE |
NDC Information of Temovate
| NDC Code | 0462-0163-30 |
| Proprietary Name | Temovate |
| Package Description | 1 TUBE in 1 CARTON (0462-0163-30) > 30 g in 1 TUBE |
| Product NDC | 0462-0163 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clobetasol propionate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19851227 |
| Marketing Category Name | NDA |
| Labeler Name | PharmaDerm A division of Fougera Pharmaceuticals Inc. |
| Substance Name | CLOBETASOL PROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
