FLUTICASONE is a Nasal Spray, Metered in the Human Prescription Drug category. It is labeled and distributed by Direct Rx. The primary component is Fluticasone Propionate.
| Product ID | 61919-611_861d65c9-fb38-b548-e053-2a91aa0a2366 |
| NDC | 61919-611 |
| Product Type | Human Prescription Drug |
| Proprietary Name | FLUTICASONE |
| Generic Name | Fluticasone |
| Dosage Form | Spray, Metered |
| Route of Administration | NASAL |
| Marketing Start Date | 2019-02-22 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076504 |
| Labeler Name | Direct RX |
| Substance Name | FLUTICASONE PROPIONATE |
| Active Ingredient Strength | 50 ug/1 |
| Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2019-04-09 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA076504 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2019-04-09 |
| Ingredient | Strength |
|---|---|
| FLUTICASONE PROPIONATE | 50 ug/1 |
| SPL SET ID: | ab7529ac-fa19-4be8-9906-8889fa3e8398 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 45865-602 | Fluticasone | Fluticasone Propionate |
| 50436-2640 | Fluticasone | Fluticasone Propionate |
| 55700-680 | FLUTICASONE | fluticasone propionate |
| 60432-264 | FLUTICASONE | fluticasone propionate |
| 61919-004 | FLUTICASONE | FLUTICASONE |
| 61919-611 | FLUTICASONE | FLUTICASONE |
| 61919-620 | FLUTICASONE | FLUTICASONE |
| 68071-1638 | Fluticasone | Fluticasone Propionate |
| 68788-7788 | FLUTICASONE | fluticasone propionate |
| 71205-443 | FLUTICASONE | fluticasone propionate |