药品名称HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER
申请号019339产品号004
活性成分HEPARIN SODIUM市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格5,000 UNITS/100ML
治疗等效代码AP参比药物
批准日期1985/03/27申请机构HOSPIRA INC
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
019339054APLetter2014/03/18下载
019339054APLabel2014/03/19下载
019339047APLabel2011/12/23下载
019339047APLetter2011/12/29下载
019339038APLetter2009/07/31下载
019339034APLetter2008/10/21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
019339054AP2014/03/13Labeling Revision
019339050AP2013/02/08Manufacturing Change or Addition
019339047AP2011/12/23Labeling Revision
019339038AP2009/07/23Labeling Revision
019339034AP2008/10/17Labeling Revision
019339025AP2002/11/07Package Change
019339024AP1999/11/19Labeling Revision
019339023AP1998/10/27Control Supplement
019339022AP1998/10/27Control Supplement
019339021AP1998/03/16Labeling Revision
019339020AP1997/06/09Manufacturing Change or Addition
019339019AP1998/05/27Labeling Revision
019339018AP1996/02/07Package Change
019339017AP1995/08/24Manufacturing Change or Addition
019339016AP1996/08/30Manufacturing Change or Addition
019339015AP1995/08/22Package Change
019339014AP1994/11/10Package Change
019339013AP1994/11/10Manufacturing Change or Addition
019339012AP1994/11/10Package Change
019339011AP1994/11/10Formulation Revision
019339009AP1992/02/25Manufacturing Change or Addition
019339008AP1992/02/18Package Change
019339006AP1990/02/16Control Supplement
019339004AP1986/10/29Formulation Revision
019339003AP1986/08/03Manufacturing Change or Addition
019339002AP1986/09/24Manufacturing Change or Addition
019339001AP1986/04/01Package Change
019339000AP1985/03/27Approval