| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1650-6 | 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 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1650-6) |
| 71335-1650-7 | 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 | 42 TABLET, FILM COATED in 1 BOTTLE (71335-1650-7) |
| 71335-1650-8 | 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 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-1650-8) |
| 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) |