| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 50090-3418-2 | 50090-3418 | HUMAN PRESCRIPTION DRUG | Methotrexate | Methotrexate Sodium | TABLET | ORAL | 20180326 | N/A | ANDA | ANDA201749 | A-S Medication Solutions | METHOTREXATE SODIUM | 2.5 mg/1 | 100 TABLET in 1 BOTTLE (50090-3418-2) |
| 72162-2174-1 | 72162-2174 | HUMAN PRESCRIPTION DRUG | Methotrexate | Methotrexate Sodium | TABLET | ORAL | 20231207 | N/A | ANDA | ANDA201749 | Bryant Ranch Prepack | METHOTREXATE SODIUM | 2.5 mg/1 | 100 TABLET in 1 BOTTLE (72162-2174-1) |
| 47335-235-83 | 47335-235 | HUMAN PRESCRIPTION DRUG | Methotrexate | Methotrexate Sodium | TABLET | ORAL | 20171110 | N/A | ANDA | ANDA201749 | Sun Pharmaceutical Industries, Inc. | METHOTREXATE SODIUM | 2.5 mg/1 | 100 TABLET in 1 BOTTLE (47335-235-83) |
| 47335-235-96 | 47335-235 | HUMAN PRESCRIPTION DRUG | Methotrexate | Methotrexate Sodium | TABLET | ORAL | 20171110 | N/A | ANDA | ANDA201749 | Sun Pharmaceutical Industries, Inc. | METHOTREXATE SODIUM | 2.5 mg/1 | 36 TABLET in 1 BOTTLE (47335-235-96) |