药品名称HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER
申请号019805产品号002
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1989/01/25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
019805036APLetter2014/03/18下载
019805036APLabel2014/03/19下载
019805029APLabel2011/12/23下载
019805029APLetter2012/01/03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
019805036AP2014/03/13Labeling Revision
019805032AP2013/02/08Manufacturing Change or Addition
019805029AP2011/12/23Labeling Revision
019805015AP2002/09/18Expiration Date Change
019805014AP2000/03/16Labeling Revision
019805013AP1997/11/25Control Supplement
019805012AP1998/05/27Labeling Revision
019805011AP1996/08/29Package Change
019805010AP1995/08/24Manufacturing Change or Addition
019805009AP1996/09/05Manufacturing Change or Addition
019805008AP1996/08/30Manufacturing Change or Addition
019805007AP1992/02/25Manufacturing Change or Addition
019805005AP1992/02/18Package Change
019805004AP1990/10/16Manufacturing Change or Addition
019805003AP1990/02/16Control Supplement
019805000AP1989/01/25Approval