美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=LOVENOX (PRESERVATIVE FREE)"
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
LOVENOX (PRESERVATIVE FREE) 020164 001 NDA ENOXAPARIN SODIUM INJECTABLE;SUBCUTANEOUS 30MG/0.3ML (100MG/ML) Yes No 1993/03/29 1993/03/29 SANOFI AVENTIS US Prescription
LOVENOX (PRESERVATIVE FREE) 020164 002 NDA ENOXAPARIN SODIUM INJECTABLE;SUBCUTANEOUS 40MG/0.4ML (100MG/ML) Yes No 1993/03/29 1998/01/30 SANOFI AVENTIS US Prescription
LOVENOX (PRESERVATIVE FREE) 020164 003 NDA ENOXAPARIN SODIUM INJECTABLE;SUBCUTANEOUS 60MG/0.6ML (100MG/ML) Yes No 1993/03/29 1998/03/27 SANOFI AVENTIS US Prescription
LOVENOX (PRESERVATIVE FREE) 020164 004 NDA ENOXAPARIN SODIUM INJECTABLE;SUBCUTANEOUS 80MG/0.8ML (100MG/ML) Yes No 1993/03/29 1998/03/27 SANOFI AVENTIS US Prescription
LOVENOX (PRESERVATIVE FREE) 020164 005 NDA ENOXAPARIN SODIUM INJECTABLE;SUBCUTANEOUS 100MG/ML (100MG/ML) Yes Yes 1993/03/29 1998/03/27 SANOFI AVENTIS US Prescription
LOVENOX (PRESERVATIVE FREE) 020164 006 NDA ENOXAPARIN SODIUM INJECTABLE;SUBCUTANEOUS 90MG/0.6ML (150MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1993/03/29 2000/06/02 SANOFI AVENTIS US Discontinued
LOVENOX (PRESERVATIVE FREE) 020164 007 NDA ENOXAPARIN SODIUM INJECTABLE;SUBCUTANEOUS 120MG/0.8ML (150MG/ML) Yes No 1993/03/29 2000/06/02 SANOFI AVENTIS US Prescription
LOVENOX (PRESERVATIVE FREE) 020164 008 NDA ENOXAPARIN SODIUM INJECTABLE;SUBCUTANEOUS 150MG/ML (150MG/ML) Yes No 1993/03/29 2000/06/02 SANOFI AVENTIS US Prescription
药品名称,活性成分,申请号搜索 高级检索
©2006-2024 DrugFuture->U.S. FDA Drugs Database