Product NDC: | 54868-5458 |
Proprietary Name: | Fluticasone Propionate |
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) |
Product NDC: | 54868-5458 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076668 |
Marketing Category: | ANDA |
Start Marketing Date: | 20051020 |
Package NDC: | 54868-5458-0 |
Package Description: | 1 TUBE in 1 CARTON (54868-5458-0) > 60 g in 1 TUBE |
NDC Code | 54868-5458-0 |
Proprietary Name | Fluticasone Propionate |
Package Description | 1 TUBE in 1 CARTON (54868-5458-0) > 60 g in 1 TUBE |
Product NDC | 54868-5458 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluticasone propionate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20051020 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | FLUTICASONE PROPIONATE |
Strength Number | .05 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |