美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CYTOXAN (LYOPHILIZED)"
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
CYTOXAN (LYOPHILIZED) 012142 003 NDA CYCLOPHOSPHAMIDE INJECTABLE;INJECTION 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1959/11/16 Approved Prior to Jan 1, 1982 BAXTER HLTHCARE Discontinued
CYTOXAN (LYOPHILIZED) 012142 004 NDA CYCLOPHOSPHAMIDE INJECTABLE;INJECTION 1GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1959/11/16 1982/08/30 BAXTER HLTHCARE Discontinued
CYTOXAN (LYOPHILIZED) 012142 005 NDA CYCLOPHOSPHAMIDE INJECTABLE;INJECTION 2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1959/11/16 1982/08/30 BAXTER HLTHCARE Discontinued
CYTOXAN (LYOPHILIZED) 012142 008 NDA CYCLOPHOSPHAMIDE INJECTABLE;INJECTION 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1959/11/16 1984/01/04 BAXTER HLTHCARE Discontinued
CYTOXAN (LYOPHILIZED) 012142 009 NDA CYCLOPHOSPHAMIDE INJECTABLE;INJECTION 2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1959/11/16 1985/12/10 BAXTER HLTHCARE Discontinued
CYTOXAN (LYOPHILIZED) 012142 010 NDA CYCLOPHOSPHAMIDE INJECTABLE;INJECTION 1GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1959/11/16 1985/09/24 BAXTER HLTHCARE Discontinued
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