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 条
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商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
DIAMOX 008943 001 NDA ACETAZOLAMIDE TABLET;ORAL 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1953/07/27 Approved Prior to Jan 1, 1982 TEVA BRANDED PHARM Discontinued
DIAMOX 008943 002 NDA ACETAZOLAMIDE TABLET;ORAL 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1953/07/27 Approved Prior to Jan 1, 1982 TEVA BRANDED PHARM Discontinued
DIAMOX 009388 001 NDA ACETAZOLAMIDE SODIUM INJECTABLE;INJECTION EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1954/06/25 Approved Prior to Jan 1, 1982 TEVA WOMENS Discontinued
DIAMOX 012945 001 NDA ACETAZOLAMIDE CAPSULE, EXTENDED RELEASE;ORAL 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1962/01/25 Approved Prior to Jan 1, 1982 TEVA BRANDED PHARM Discontinued
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