| Product NDC: | 52125-615 |
| Proprietary Name: | VERAMYST |
| Non Proprietary Name: | fluticasone furoate |
| Active Ingredient(s): | 27.5 ug/1 & nbsp; fluticasone furoate |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52125-615 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022051 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130607 |
| Package NDC: | 52125-615-01 |
| Package Description: | 120 SPRAY, METERED in 1 BOTTLE, PUMP (52125-615-01) |
| NDC Code | 52125-615-01 |
| Proprietary Name | VERAMYST |
| Package Description | 120 SPRAY, METERED in 1 BOTTLE, PUMP (52125-615-01) |
| Product NDC | 52125-615 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluticasone furoate |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20130607 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | FLUTICASONE FUROATE |
| Strength Number | 27.5 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |