POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER(CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE)

药品名称	POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
申请号	019367	产品号	005
活性成分	CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE	市场状态	处方药
剂型或给药途径	INJECTABLE;INJECTION	规格	20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML
治疗等效代码	AP	参比药物	否
批准日期	1985/04/05	申请机构	BAXTER HEALTHCARE CORP
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
019367	031	AP	2014/09/30	Manufacturing Change or Addition
019367	029	AP	2013/04/26	Manufacturing Change or Addition
019367	026	AP	2011/10/19	Labeling Revision
019367	022	AP	2005/08/26	Package Change
019367	021	AP	2005/06/07	Labeling Revision
019367	016	AP	2001/08/14	Manufacturing Change or Addition
019367	015	AP	2003/01/03	Labeling Revision
019367	014	AP	1999/11/24	Manufacturing Change or Addition
019367	013	AP	1997/04/29	Package Change
019367	012	AP	1994/02/18	Control Supplement
019367	011	AP	1994/09/30	Control Supplement
019367	010	AP	1991/12/11	Control Supplement
019367	008	AP	1991/04/29	Control Supplement
019367	007	AP	1991/03/26	Control Supplement
019367	006	AP	1991/02/15	Control Supplement
019367	005	AP	1989/07/26	Control Supplement
019367	003	AP	1987/07/25	Package Change
019367	002	AP	1987/05/28	Control Supplement
019367	000	AP	1985/04/05	Approval