| Product NDC: | 68462-427 |
| 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) |
| Product NDC: | 68462-427 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090759 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111013 |
| Package NDC: | 68462-427-02 |
| Package Description: | 1 BOTTLE in 1 CARTON (68462-427-02) > 60 mL in 1 BOTTLE |
| NDC Code | 68462-427-02 |
| Proprietary Name | Fluticasone Propionate |
| Package Description | 1 BOTTLE in 1 CARTON (68462-427-02) > 60 mL in 1 BOTTLE |
| Product NDC | 68462-427 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluticasone Propionate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111013 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc., USA |
| Substance Name | FLUTICASONE PROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |