美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ELOXATIN"
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
ELOXATIN 021492 001 NDA OXALIPLATIN INJECTABLE;INTRAVENOUS 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 2002/08/09 2002/08/09 SANOFI AVENTIS US Discontinued
ELOXATIN 021492 002 NDA OXALIPLATIN INJECTABLE;INTRAVENOUS 100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 2002/08/09 2002/08/09 SANOFI AVENTIS US Discontinued
ELOXATIN 021759 001 NDA OXALIPLATIN INJECTABLE;INTRAVENOUS 50MG/10ML (5MG/ML) Yes Yes 2005/01/31 2005/01/31 SANOFI AVENTIS US Prescription
ELOXATIN 021759 002 NDA OXALIPLATIN INJECTABLE;INTRAVENOUS 100MG/20ML (5MG/ML) Yes Yes 2005/01/31 2005/01/31 SANOFI AVENTIS US Prescription
ELOXATIN 021759 003 NDA OXALIPLATIN INJECTABLE;INTRAVENOUS 200MG/40ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 2005/01/31 2006/11/17 SANOFI AVENTIS US Discontinued
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