共 1 页 当前第 1 页 返回检索页| 1 | 药品名称 | IMDUR |
| 申请号 | 020225 | 产品号 | 001 |
| 活性成分 | ISOSORBIDE MONONITRATE | 市场状态 | 停止上市 |
| 剂型或给药途径 | TABLET, EXTENDED RELEASE;ORAL | 规格 | 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |
| 治疗等效代码 | | 参比药物 | 否 |
| 批准日期 | 1993/08/12 | 申请机构 | SCHERING PLOUGH CORP
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| 2 | 药品名称 | IMDUR |
| 申请号 | 020225 | 产品号 | 002 |
| 活性成分 | ISOSORBIDE MONONITRATE | 市场状态 | 停止上市 |
| 剂型或给药途径 | TABLET, EXTENDED RELEASE;ORAL | 规格 | 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |
| 治疗等效代码 | | 参比药物 | 否 |
| 批准日期 | 1993/08/12 | 申请机构 | SCHERING PLOUGH CORP
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| 3 | 药品名称 | IMDUR |
| 申请号 | 020225 | 产品号 | 003 |
| 活性成分 | ISOSORBIDE MONONITRATE | 市场状态 | 停止上市 |
| 剂型或给药途径 | TABLET, EXTENDED RELEASE;ORAL | 规格 | 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |
| 治疗等效代码 | | 参比药物 | 否 |
| 批准日期 | 1995/03/30 | 申请机构 | SCHERING PLOUGH CORP
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