| NDC包装代码 | 产品NDC | 产品类型 | 商品名 | 通用名 | 剂型 | 给药途径 | 上市日期 | 结束日期 | 市场类别 | 申请号 | 标签持有者 | 活性成分 | 规格 | 包装描述 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1650-9 | 71335-1650 | HUMAN PRESCRIPTION DRUG | Naproxen sodium | Naproxen sodium | TABLET, FILM COATED | ORAL | 20240812 | N/A | ANDA | ANDA078486 | Bryant Ranch Prepack | NAPROXEN SODIUM | 550 mg/1 | 56 TABLET, FILM COATED in 1 BOTTLE (71335-1650-9) |
| 85509-1495-3 | 85509-1495 | HUMAN PRESCRIPTION DRUG | Naproxen sodium | Naproxen sodium | TABLET, FILM COATED | ORAL | 20260107 | N/A | ANDA | ANDA078486 | PHOENIX RX LLC | NAPROXEN SODIUM | 550 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (85509-1495-3) |
| 85509-1495-6 | 85509-1495 | HUMAN PRESCRIPTION DRUG | Naproxen sodium | Naproxen sodium | TABLET, FILM COATED | ORAL | 20260107 | N/A | ANDA | ANDA078486 | PHOENIX RX LLC | NAPROXEN SODIUM | 550 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (85509-1495-6) |
| 85509-1495-9 | 85509-1495 | HUMAN PRESCRIPTION DRUG | Naproxen sodium | Naproxen sodium | TABLET, FILM COATED | ORAL | 20260107 | N/A | ANDA | ANDA078486 | PHOENIX RX LLC | NAPROXEN SODIUM | 550 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (85509-1495-9) |