美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=DANOCRINE"
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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
DANOCRINE 017557 002 NDA DANAZOL CAPSULE;ORAL 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1976/06/21 Approved Prior to Jan 1, 1982 SANOFI AVENTIS US Discontinued
DANOCRINE 017557 003 NDA DANAZOL CAPSULE;ORAL 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1976/06/21 Approved Prior to Jan 1, 1982 SANOFI AVENTIS US Discontinued
DANOCRINE 017557 004 NDA DANAZOL CAPSULE;ORAL 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1976/06/21 Approved Prior to Jan 1, 1982 SANOFI AVENTIS US Discontinued
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