美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CLAFORAN"
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
CLAFORAN 050547 001 NDA CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1981/03/11 Approved Prior to Jan 1, 1982 STERIMAX Discontinued
CLAFORAN 050547 002 NDA CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1981/03/11 Approved Prior to Jan 1, 1982 STERIMAX Discontinued
CLAFORAN 050547 003 NDA CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1981/03/11 Approved Prior to Jan 1, 1982 STERIMAX Discontinued
CLAFORAN 050547 004 NDA CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1981/03/11 1983/12/29 STERIMAX Discontinued
CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER 050596 001 NDA CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 20MG BASE/ML No No 1985/05/20 1985/05/20 STERIMAX Discontinued
CLAFORAN IN DEXTROSE 5% IN PLASTIC CONTAINER 050596 002 NDA CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 20MG BASE/ML No No 1985/05/20 1985/05/20 STERIMAX Discontinued
CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER 050596 003 NDA CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 40MG BASE/ML No No 1985/05/20 1985/05/20 STERIMAX Discontinued
CLAFORAN IN DEXTROSE 5% IN PLASTIC CONTAINER 050596 004 NDA CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 40MG BASE/ML No No 1985/05/20 1985/05/20 STERIMAX Discontinued
CLAFORAN 062659 001 ANDA CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 1GM BASE/VIAL No No 1987/01/13 1987/01/13 SANOFI AVENTIS US Discontinued
CLAFORAN 062659 002 ANDA CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 2GM BASE/VIAL No No 1987/01/13 1987/01/13 SANOFI AVENTIS US Discontinued
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