PLASMA-LYTE A IN PLASTIC CONTAINER(MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE)

药品名称	PLASMA-LYTE A IN PLASTIC CONTAINER
申请号	017378	产品号	002
活性成分	MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE	市场状态	处方药
剂型或给药途径	INJECTABLE;INJECTION	规格	30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML
治疗等效代码	AP	参比药物	否
批准日期	1982/11/22	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

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
017378	068	AP	Letter	2013/09/13	下载
017378	068	AP	Label	2013/09/17	下载
017378	065	AP	Letter	2009/01/30	下载
017378	065	AP	Label	2009/02/04	下载
017378	055	AP	Letter	2002/04/03	下载

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
017378	072	AP	2016/04/28	Manufacturing Change or Addition
017378	071	AP	2016/01/26	Manufacturing Change or Addition
017378	069	AP	2015/02/03	Manufacturing Change or Addition
017378	068	AP	2013/09/11	Labeling Revision
017378	065	AP	2009/01/27	Labeling Revision
017378	059	AP	2001/08/14	Manufacturing Change or Addition
017378	058	AP	2001/02/01	Labeling Revision
017378	057	AP	1999/11/24	Manufacturing Change or Addition
017378	056	AP	1999/02/04	Control Supplement
017378	055	AP	2002/04/03	Labeling Revision
017378	054	AP	1997/04/29	Package Change
017378	053	AP	1994/02/18	Control Supplement
017378	052	AP	1994/09/30	Control Supplement
017378	050	AP	1991/04/29	Control Supplement
017378	049	AP	1990/05/24	Control Supplement
017378	048	AP	1991/03/26	Control Supplement
017378	047	AP	1991/02/15	Control Supplement
017378	046	AP	1989/07/26	Control Supplement
017378	045	AP	1987/07/25	Package Change
017378	044	AP	1987/05/28	Control Supplement
017378	042	AP	1986/02/27	Package Change
017378	041	AP	1985/04/15	Control Supplement
017378	040	AP	1985/01/26	Labeling Revision
017378	039	AP	1985/06/13	Control Supplement
017378	038	AP	1984/09/22	Control Supplement
017378	036	AP	1984/02/28	Control Supplement
017378	035	AP	1985/01/19	Labeling Revision
017378	033	AP	1985/08/28	Control Supplement
017378	032	AP	1985/08/28	Control Supplement
017378	031	AP	1984/03/16	Control Supplement
017378	030	AP	1982/11/22	Labeling Revision
017378	029	AP	1982/11/22	Control Supplement
017378	028	AP	1985/01/24	Control Supplement
017378	026	AP	1982/02/16	Control Supplement
017378	025	AP	1983/07/11	Practioner Draft Labeling
017378	024	AP	1983/07/11	Practioner Draft Labeling
017378	023	AP	1981/11/20	Control Supplement
017378	021	AP	1982/06/03	Control Supplement
017378	020	AP	1982/04/16	Control Supplement
017378	019	AP	1981/08/26	Labeling Revision
017378	018	AP	1981/12/21	Control Supplement
017378	017	AP	1981/09/03	Labeling Revision
017378	016	AP	1981/09/03	Control Supplement
017378	014	AP	1981/06/29	Control Supplement
017378	013	AP	1981/01/21	Control Supplement
017378	012	AP	1980/07/31	Control Supplement
017378	011	AP	1981/04/16	Control Supplement
017378	009	AP	1980/06/18	Control Supplement
017378	007	AP	1980/05/30	Control Supplement
017378	006	AP	1980/08/07	Control Supplement
017378	005	AP	1979/08/02	Control Supplement
017378	003	AP	1980/06/28	Control Supplement
017378	002	AP	1979/06/14	Control Supplement
017378	001	AP	1980/02/25	Control Supplement
017378	000	AP	1979/02/02	Approval

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