共 1 页 当前第 1 页 返回检索页| 1 | 药品名称 | ZEFAZONE |
| 申请号 | 050637 | 产品号 | 001 |
| 活性成分 | CEFMETAZOLE SODIUM | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1989/12/11 | 申请机构 | PHARMACIA AND UPJOHN CO
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| 2 | 药品名称 | ZEFAZONE |
| 申请号 | 050637 | 产品号 | 002 |
| 活性成分 | CEFMETAZOLE SODIUM | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1989/12/11 | 申请机构 | PHARMACIA AND UPJOHN CO
|
| 3 | 药品名称 | ZEFAZONE IN PLASTIC CONTAINER |
| 申请号 | 050683 | 产品号 | 001 |
| 活性成分 | CEFMETAZOLE SODIUM | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1992/12/29 | 申请机构 | PHARMACIA AND UPJOHN CO
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| 4 | 药品名称 | ZEFAZONE IN PLASTIC CONTAINER |
| 申请号 | 050683 | 产品号 | 002 |
| 活性成分 | CEFMETAZOLE SODIUM | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1992/12/29 | 申请机构 | PHARMACIA AND UPJOHN CO
|