共 1 页 当前第 1 页 返回检索页1 | 药品名称 | SERZONE |
| 申请号 | 020152 | 产品号 | 001 |
活性成分 | NEFAZODONE HYDROCHLORIDE | 市场状态 | 停止上市 |
剂型或给药途径 | TABLET;ORAL | 规格 | 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1994/12/22 | 申请机构 | BRISTOL MYERS SQUIBB CO PHARMACEUTICAL RESEARCH INSTITUTE
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2 | 药品名称 | SERZONE |
| 申请号 | 020152 | 产品号 | 002 |
活性成分 | NEFAZODONE HYDROCHLORIDE | 市场状态 | 停止上市 |
剂型或给药途径 | TABLET;ORAL | 规格 | 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1994/12/22 | 申请机构 | BRISTOL MYERS SQUIBB CO PHARMACEUTICAL RESEARCH INSTITUTE
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3 | 药品名称 | SERZONE |
| 申请号 | 020152 | 产品号 | 003 |
活性成分 | NEFAZODONE HYDROCHLORIDE | 市场状态 | 停止上市 |
剂型或给药途径 | TABLET;ORAL | 规格 | 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1994/12/22 | 申请机构 | BRISTOL MYERS SQUIBB CO PHARMACEUTICAL RESEARCH INSTITUTE
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4 | 药品名称 | SERZONE |
| 申请号 | 020152 | 产品号 | 004 |
活性成分 | NEFAZODONE HYDROCHLORIDE | 市场状态 | 停止上市 |
剂型或给药途径 | TABLET;ORAL | 规格 | 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1994/12/22 | 申请机构 | BRISTOL MYERS SQUIBB CO PHARMACEUTICAL RESEARCH INSTITUTE
|
5 | 药品名称 | SERZONE |
| 申请号 | 020152 | 产品号 | 005 |
活性成分 | NEFAZODONE HYDROCHLORIDE | 市场状态 | 停止上市 |
剂型或给药途径 | TABLET;ORAL | 规格 | 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1994/12/22 | 申请机构 | BRISTOL MYERS SQUIBB CO PHARMACEUTICAL RESEARCH INSTITUTE
|
6 | 药品名称 | SERZONE |
| 申请号 | 020152 | 产品号 | 006 |
活性成分 | NEFAZODONE HYDROCHLORIDE | 市场状态 | 停止上市 |
剂型或给药途径 | TABLET;ORAL | 规格 | 300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1994/12/22 | 申请机构 | BRISTOL MYERS SQUIBB CO PHARMACEUTICAL RESEARCH INSTITUTE
|