AMINOSYN II 3.5% W/ ELECTROLYTES IN DEXTROSE 25% W/ CALCIUM IN PLASTIC CONTAINER(AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE)

药品名称	AMINOSYN II 3.5% W/ ELECTROLYTES IN DEXTROSE 25% W/ CALCIUM IN PLASTIC CONTAINER
申请号	019683	产品号	001
活性成分	AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE	市场状态	停止上市
剂型或给药途径	INJECTABLE;INJECTION	规格	3.5%;36.8MG/100ML;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML
治疗等效代码		参比药物	否
批准日期	1988/11/07	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
019683	027	AP	2005/10/05	Labeling Revision
019683	021	AP	2003/01/31	Control Supplement
019683	020	AP	2002/11/08	Control Supplement
019683	019	AP	2003/05/19	Labeling Revision
019683	018	AP	1998/10/29	Control Supplement
019683	017	AP	1998/12/29	Control Supplement
019683	015	AP	1997/08/20	Control Supplement
019683	014	AP	1997/06/11	Manufacturing Change or Addition
019683	013	AP	1997/05/05	Control Supplement
019683	012	AP	1996/03/04	Control Supplement
019683	011	AP	1997/03/04	Control Supplement
019683	010	AP	1995/08/18	Manufacturing Change or Addition
019683	009	AP	1996/08/27	Control Supplement
019683	008	AP	1994/07/11	Manufacturing Change or Addition
019683	006	AP	1993/12/30	Control Supplement
019683	005	AP	1992/09/28	Manufacturing Change or Addition
019683	004	AP	1991/08/30	Package Change
019683	003	AP	1992/01/28	Package Change
019683	002	AP	1992/08/18	Manufacturing Change or Addition
019683	001	AP	1990/01/11	Manufacturing Change or Addition
019683	000	AP	1988/11/07	Approval