药品名称HEPARIN SODIUM 10,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER
申请号018814产品号002
活性成分HEPARIN SODIUM市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格2,000 UNITS/100ML
治疗等效代码参比药物
批准日期1985/07/09申请机构BAXTER HEALTHCARE CORP
化学类型New formulation or new manufacturer审评分类Standard review drug
与本品相关的专利信息(来自橙皮书Orange Book)
专利号专利过期日是否化合物专利是否产品专利专利用途代码专利下载
历史专利信息
与本品相关的市场独占权保护信息
独占权代码失效日期
历史市场独占权保护信息
与药品注册相关的信息
申请号修订号审批结论公开文档类型文档创建时间获取文档
018814032APLetter2010/08/20下载
018814032APLabel2010/08/28下载
药品注册审批历史信息
申请号修订号审批结论审批日期审批内容
018814032AP2010/08/13Labeling Revision
018814027AP1999/11/23Package Change
018814026AP2000/10/19Labeling Revision
018814025AP1999/06/01Manufacturing Change or Addition
018814024AP2000/02/04Labeling Revision
018814022AP1996/09/17Labeling Revision
018814021AP1994/03/10Control Supplement
018814020AP1994/09/14Manufacturing Change or Addition
018814019AP1994/07/20Formulation Revision
018814018AP1994/07/20Package Change
018814017AP1993/04/15Manufacturing Change or Addition
018814015AP1991/07/16Manufacturing Change or Addition
018814013AP1992/11/19Labeling Revision
018814012AP1991/03/04Control Supplement
018814011AP1991/04/25Control Supplement
018814010AP1989/08/24Control Supplement
018814009AP1988/02/19Labeling Revision
018814008AP1987/07/08Package Change
018814007AP1985/10/08Control Supplement
018814006AP1985/07/09General Efficacy (MarkIV)
018814005AP1985/06/17Package Change
018814004AP1985/01/31Labeling Revision
018814002AP1984/10/16Control Supplement
018814001AP1984/06/08Control Supplement
018814000AP1983/10/31Approval