Product NDC: | 10337-434 |
Proprietary Name: | Cutivate |
Non Proprietary Name: | fluticasone propionate |
Active Ingredient(s): | .5 mg/mL & nbsp; fluticasone propionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10337-434 |
Labeler Name: | PharmaDerm, A division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021152 |
Marketing Category: | NDA |
Start Marketing Date: | 20091005 |
Package NDC: | 10337-434-07 |
Package Description: | 7 mL in 1 BOTTLE (10337-434-07) |
NDC Code | 10337-434-07 |
Proprietary Name | Cutivate |
Package Description | 7 mL in 1 BOTTLE (10337-434-07) |
Product NDC | 10337-434 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluticasone propionate |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20091005 |
Marketing Category Name | NDA |
Labeler Name | PharmaDerm, A division of Fougera Pharmaceuticals Inc. |
Substance Name | FLUTICASONE PROPIONATE |
Strength Number | .5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |