共 1 页 当前第 1 页 返回检索页| 1 | 药品名称 | DIAMOX |
| 申请号 | 008943 | 产品号 | 001 |
| 活性成分 | ACETAZOLAMIDE | 市场状态 | 停止上市 |
| 剂型或给药途径 | TABLET;ORAL | 规格 | 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | Approved Prior to Jan 1, 1982 | 申请机构 | TEVA BRANDED PHARMACEUTICAL PRODUCTS R AND D INC
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| 2 | 药品名称 | DIAMOX |
| 申请号 | 008943 | 产品号 | 002 |
| 活性成分 | ACETAZOLAMIDE | 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| 剂型或给药途径 | TABLET;ORAL | 规格 | 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | Approved Prior to Jan 1, 1982 | 申请机构 | TEVA BRANDED PHARMACEUTICAL PRODUCTS R AND D INC
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| 3 | 药品名称 | DIAMOX |
| 申请号 | 009388 | 产品号 | 001 |
| 活性成分 | ACETAZOLAMIDE SODIUM | 市场状态 | 停止上市 |
| 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** |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 | 1990/12/05 | 申请机构 | TEVA WOMENS HEALTH INC
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| 4 | 药品名称 | DIAMOX |
| 申请号 | 012945 | 产品号 | 001 |
| 活性成分 | ACETAZOLAMIDE | 市场状态 | 处方药 |
| 剂型或给药途径 | CAPSULE, EXTENDED RELEASE;ORAL | 规格 | 500MG |
| 治疗等效代码 | AB | 参比药物 | 是 |
| 批准日期 | Approved Prior to Jan 1, 1982 | 申请机构 | TEVA BRANDED PHARMACEUTICAL PRODUCTS R AND D INC
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