美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件: 药品名称=DIAMOX
符合检索条件的记录共4
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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剂型或给药途径TABLET;ORAL规格125MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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
批准日期Approved Prior to Jan 1, 1982申请机构TEVA BRANDED PHARMACEUTICAL PRODUCTS R AND D INC
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剂型或给药途径TABLET;ORAL规格250MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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
批准日期Approved Prior to Jan 1, 1982申请机构TEVA BRANDED PHARMACEUTICAL PRODUCTS R AND D INC
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剂型或给药途径INJECTABLE;INJECTION规格EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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
批准日期1990/12/05申请机构TEVA WOMENS HEALTH INC
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
批准日期Approved Prior to Jan 1, 1982申请机构TEVA BRANDED PHARMACEUTICAL PRODUCTS R AND D INC