HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER(HEPARIN SODIUM)

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	否
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
无
历史专利信息
无

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
019339	054	AP	2014/03/13	Labeling Revision
019339	050	AP	2013/02/08	Manufacturing Change or Addition
019339	047	AP	2011/12/23	Labeling Revision
019339	038	AP	2009/07/23	Labeling Revision
019339	034	AP	2008/10/17	Labeling Revision
019339	025	AP	2002/11/07	Package Change
019339	024	AP	1999/11/19	Labeling Revision
019339	023	AP	1998/10/27	Control Supplement
019339	022	AP	1998/10/27	Control Supplement
019339	021	AP	1998/03/16	Labeling Revision
019339	020	AP	1997/06/09	Manufacturing Change or Addition
019339	019	AP	1998/05/27	Labeling Revision
019339	018	AP	1996/02/07	Package Change
019339	017	AP	1995/08/24	Manufacturing Change or Addition
019339	016	AP	1996/08/30	Manufacturing Change or Addition
019339	015	AP	1995/08/22	Package Change
019339	014	AP	1994/11/10	Package Change
019339	013	AP	1994/11/10	Manufacturing Change or Addition
019339	012	AP	1994/11/10	Package Change
019339	011	AP	1994/11/10	Formulation Revision
019339	009	AP	1992/02/25	Manufacturing Change or Addition
019339	008	AP	1992/02/18	Package Change
019339	006	AP	1990/02/16	Control Supplement
019339	004	AP	1986/10/29	Formulation Revision
019339	003	AP	1986/08/03	Manufacturing Change or Addition
019339	002	AP	1986/09/24	Manufacturing Change or Addition
019339	001	AP	1986/04/01	Package Change
019339	000	AP	1985/03/27	Approval