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FLUTICASONE PROPIONATE
FLUTICASONE PROPIONATE - 0168-0434-04 - (fluticasone propionate)
Drug Information of FLUTICASONE PROPIONATE
| Product NDC: | 0168-0434 |
| Proprietary Name: | FLUTICASONE PROPIONATE |
| 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) |
Labeler Information of FLUTICASONE PROPIONATE
| Product NDC: | 0168-0434 |
| Labeler Name: | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021152 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20091005 |
Package Information of FLUTICASONE PROPIONATE
| Package NDC: | 0168-0434-04 |
| Package Description: | 1 BOTTLE in 1 CARTON (0168-0434-04) > 120 mL in 1 BOTTLE |
NDC Information of FLUTICASONE PROPIONATE
| NDC Code | 0168-0434-04 |
| Proprietary Name | FLUTICASONE PROPIONATE |
| Package Description | 1 BOTTLE in 1 CARTON (0168-0434-04) > 120 mL in 1 BOTTLE |
| Product NDC | 0168-0434 |
| 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 AUTHORIZED GENERIC |
| Labeler Name | E. Fougera & Co. 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] |
