| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0228-2620-11 | 0228-2620 | HUMAN PRESCRIPTION DRUG | Isosorbide Mononitrate | Isosorbide Mononitrate | TABLET | ORAL | 19981030 | N/A | ANDA | ANDA075037 | Actavis Pharma, Inc. | ISOSORBIDE MONONITRATE | 20 mg/1 | 100 TABLET in 1 BOTTLE (0228-2620-11) |
| 0228-2631-11 | 0228-2631 | HUMAN PRESCRIPTION DRUG | Isosorbide Mononitrate | Isosorbide Mononitrate | TABLET | ORAL | 19981030 | N/A | ANDA | ANDA075037 | Actavis Pharma, Inc. | ISOSORBIDE MONONITRATE | 10 mg/1 | 100 TABLET in 1 BOTTLE (0228-2631-11) |
| 70518-1485-1 | 70518-1485 | HUMAN PRESCRIPTION DRUG | Isosorbide Mononitrate | Isosorbide Mononitrate | TABLET | ORAL | 20200107 | N/A | ANDA | ANDA075037 | REMEDYREPACK INC. | ISOSORBIDE MONONITRATE | 10 mg/1 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1485-1) |