Product NDC: | 0462-0332 |
Proprietary Name: | Cutivate |
Non Proprietary Name: | fluticasone propionate |
Active Ingredient(s): | .5 mg/g & nbsp; fluticasone propionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0462-0332 |
Labeler Name: | PHARMADERM., A division of Nycomed US Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076451 |
Marketing Category: | ANDA |
Start Marketing Date: | 19901218 |
Package NDC: | 0462-0332-60 |
Package Description: | 60 g in 1 TUBE (0462-0332-60) |
NDC Code | 0462-0332-60 |
Proprietary Name | Cutivate |
Package Description | 60 g in 1 TUBE (0462-0332-60) |
Product NDC | 0462-0332 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluticasone propionate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19901218 |
Marketing Category Name | ANDA |
Labeler Name | PHARMADERM., A division of Nycomed US Inc. |
Substance Name | FLUTICASONE PROPIONATE |
Strength Number | .5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |