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Cutivate
Cutivate - 0462-0333-30 - (fluticasone propionate)
Drug Information of Cutivate
| Product NDC: | 0462-0333 |
| Proprietary Name: | Cutivate |
| Non Proprietary Name: | fluticasone propionate |
| Active Ingredient(s): | .05 mg/g & nbsp; fluticasone propionate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cutivate
| Product NDC: | 0462-0333 |
| Labeler Name: | PharmaDerm a division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019957 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19901214 |
Package Information of Cutivate
| Package NDC: | 0462-0333-30 |
| Package Description: | 30 g in 1 TUBE (0462-0333-30) |
NDC Information of Cutivate
| NDC Code | 0462-0333-30 |
| Proprietary Name | Cutivate |
| Package Description | 30 g in 1 TUBE (0462-0333-30) |
| Product NDC | 0462-0333 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluticasone propionate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19901214 |
| Marketing Category Name | NDA |
| Labeler Name | PharmaDerm a division of Fougera Pharmaceuticals Inc. |
| Substance Name | FLUTICASONE PROPIONATE |
| Strength Number | .05 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
