POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.225% IN PLASTIC CONTAINER(DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)

药品名称	POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.225% IN PLASTIC CONTAINER
申请号	018365	产品号	009
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;298MG/100ML;225MG/100ML
治疗等效代码		参比药物	否
批准日期	1988/03/28	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

与本品相关的市场独占权保护信息
独占权代码	失效日期
无
历史市场独占权保护信息
无

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
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
018365	091	AP	2013/09/05	Manufacturing Change or Addition
018365	070	AP	2001/08/24	Labeling Revision
018365	069	AP	1999/01/22	Control Supplement
018365	068	AP	1998/10/29	Control Supplement
018365	066	AP	1997/06/11	Manufacturing Change or Addition
018365	065	AP	1997/08/20	Labeling Revision
018365	064	AP	1996/08/06	Control Supplement
018365	063	AP	1996/03/04	Control Supplement
018365	062	AP	1995/08/18	Manufacturing Change or Addition
018365	061	AP	1996/08/29	Control Supplement
018365	060	AP	1996/08/27	Control Supplement
018365	059	AP	1995/08/14	Control Supplement
018365	056	AP	1991/08/30	Package Change
018365	055	AP	1992/01/28	Package Change
018365	054	AP	1991/09/10	Control Supplement
018365	052	AP	1990/01/11	Manufacturing Change or Addition
018365	051	AP	1990/02/22	Manufacturing Change or Addition
018365	049	AP	1988/03/28	Labeling Revision
018365	048	AP	1988/03/28	Control Supplement
018365	046	AP	1986/11/26	Control Supplement
018365	045	AP	1986/08/08	Control Supplement
018365	044	AP	1986/01/31	Control Supplement
018365	043	AP	1985/06/10	Control Supplement
018365	042	AP	1986/01/31	Control Supplement
018365	040	AP	1985/10/26	Labeling Revision
018365	039	AP	1985/05/03	Control Supplement
018365	038	AP	1985/10/26	Control Supplement
018365	037	AP	1984/11/09	Resubmission - Chemistry (MarkIV)
018365	034	AP	1984/10/22	Control Supplement
018365	033	AP	1985/09/26	Package Change
018365	031	AP	1985/11/29	Labeling Revision
018365	030	AP	1985/11/29	Control Supplement
018365	029	AP	1985/10/29	Package Change
018365	028	AP	1984/11/28	Control Supplement
018365	027	AP	1989/06/22	Control Supplement
018365	026	AP	1984/04/09	Control Supplement
018365	025	AP	1984/10/17	Control Supplement
018365	024	AP	1984/03/21	Control Supplement
018365	023	AP	1983/07/05	Labeling Revision
018365	022	AP	1983/07/05	Control Supplement
018365	021	AP	1983/12/08	Control Supplement
018365	020	AP	1984/02/17	Control Supplement
018365	019	AP	1984/10/10	Labeling Revision
018365	018	AP	1984/10/10	Package Change
018365	017	AP	1982/07/26	Control Supplement
018365	016	AP	1984/03/01	Control Supplement
018365	015	AP	1983/02/15	Manufacturing Change or Addition
018365	014	AP	1982/06/18	Control Supplement
018365	013	AP	1982/07/08	Control Supplement
018365	012	AP	1982/02/01	Control Supplement
018365	011	AP	1982/01/08	Control Supplement
018365	010	AP	1982/06/09	Control Supplement
018365	009	AP	1981/10/07	Control Supplement
018365	008	AP	1981/07/27	Labeling Revision
018365	006	AP	1981/06/20	Practioner Draft Labeling
018365	005	AP	1981/04/08	Labeling Revision
018365	004	AP	1981/04/08	Control Supplement
018365	003	AP	1981/01/07	Control Supplement
018365	002	AP	1980/09/15	Control Supplement
018365	001	AP	1980/08/13	Control Supplement
018365	000	AP	1980/05/29	Approval

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