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Fluticasone Propionate
Fluticasone Propionate - 0168-0333-30 - (fluticasone propionate)
Drug Information of Fluticasone Propionate
| Product NDC: | 0168-0333 |
| 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) |
Labeler Information of Fluticasone Propionate
| Product NDC: | 0168-0333 |
| Labeler Name: | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076300 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040514 |
Package Information of Fluticasone Propionate
| Package NDC: | 0168-0333-30 |
| Package Description: | 30 g in 1 TUBE (0168-0333-30) |
NDC Information of Fluticasone Propionate
| NDC Code | 0168-0333-30 |
| Proprietary Name | Fluticasone Propionate |
| Package Description | 30 g in 1 TUBE (0168-0333-30) |
| Product NDC | 0168-0333 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluticasone propionate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20040514 |
| Marketing Category Name | ANDA |
| Labeler Name | E. FOUGERA & CO. 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] |
