POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER(DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)

药品名称	POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
申请号	018876	产品号	003
活性成分	DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	市场状态	处方药
剂型或给药途径	INJECTABLE;INJECTION	规格	5GM/100ML;224MG/100ML;300MG/100ML
治疗等效代码		参比药物	否
批准日期	1986/01/17	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
018876	045	AP	2013/09/05	Manufacturing Change or Addition
018876	024	AP	2001/08/24	Labeling Revision
018876	023	AP	1998/10/29	Control Supplement
018876	021	AP	1997/06/11	Manufacturing Change or Addition
018876	020	AP	1997/08/20	Labeling Revision
018876	019	AP	1996/08/06	Control Supplement
018876	018	AP	1996/03/04	Control Supplement
018876	017	AP	1995/08/18	Manufacturing Change or Addition
018876	016	AP	1996/08/29	Control Supplement
018876	015	AP	1996/08/27	Control Supplement
018876	013	AP	1992/01/28	Package Change
018876	012	AP	1991/09/10	Control Supplement
018876	010	AP	1990/01/11	Manufacturing Change or Addition
018876	009	AP	1990/02/22	Manufacturing Change or Addition
018876	007	AP	1987/08/31	Expiration Date Change
018876	006	AP	1988/03/28	Labeling Revision
018876	005	AP	1988/03/28	Control Supplement
018876	003	AP	1989/06/22	Control Supplement
018876	002	AP	1986/08/11	Control Supplement
018876	001	AP	1986/10/09	Control Supplement
018876	000	AP	1986/01/17	Approval