DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 40MEQ(DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)

药品名称	DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 40MEQ
申请号	018037	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;300MG/100ML;200MG/100ML
治疗等效代码	AP	参比药物	否
批准日期	1982/04/13	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
018037	070	AP	Label	2013/09/11	下载
018037	070	AP	Letter	2013/09/12	下载
018037	066	AP	Label	2007/04/25	下载
018037	066	AP	Letter	2007/05/01	下载
018037	065	AP	Letter	2005/08/31	下载
018037	065	AP	Label	2005/08/31	下载
018037	063	AP	Letter	2004/06/07	下载
018037	059	AP	Letter	2003/05/29	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
018037	070	AP	2013/09/10	Labeling Revision
018037	066	AP	2007/04/20	Labeling Revision
018037	065	AP	2005/08/26	Package Change
018037	063	AP	2004/06/02	Labeling Revision
018037	060	AP	2001/08/14	Manufacturing Change or Addition
018037	059	AP	2003/04/14	Labeling Revision
018037	058	AP	1999/11/24	Manufacturing Change or Addition
018037	057	AP	1997/04/29	Package Change
018037	056	AP	1994/02/18	Control Supplement
018037	055	AP	1994/09/30	Control Supplement
018037	054	AP	1991/12/11	Control Supplement
018037	052	AP	1991/04/29	Control Supplement
018037	051	AP	1991/03/26	Control Supplement
018037	050	AP	1991/02/15	Control Supplement
018037	049	AP	1989/07/26	Control Supplement
018037	048	AP	1987/07/25	Package Change
018037	047	AP	1987/05/28	Control Supplement
018037	044	AP	1986/02/27	Package Change
018037	043	AP	1985/04/15	Control Supplement
018037	042	AP	1985/07/03	Labeling Revision
018037	041	AP	1985/06/13	Control Supplement
018037	040	AP	1984/10/23	Control Supplement
018037	039	AP	1984/02/28	Control Supplement
018037	037	AP	1985/08/28	Control Supplement
018037	036	AP	1985/08/28	Control Supplement
018037	035	AP	1984/03/16	Control Supplement
018037	034	AP	1985/01/24	Control Supplement
018037	032	AP	1982/05/25	Labeling Revision
018037	031	AP	1982/04/13	Labeling Revision
018037	029	AP	1983/07/11	Practioner Draft Labeling
018037	028	AP	1981/11/20	Control Supplement
018037	026	AP	1982/06/03	Control Supplement
018037	025	AP	1981/11/09	Control Supplement
018037	024	AP	1982/04/16	Control Supplement
018037	023	AP	1981/08/26	Labeling Revision
018037	022	AP	1981/12/21	Control Supplement
018037	020	AP	1981/06/29	Control Supplement
018037	019	AP	1981/05/29	Control Supplement
018037	018	AP	1981/01/21	Control Supplement
018037	017	AP	1980/07/31	Control Supplement
018037	014	AP	1980/08/06	Control Supplement
018037	013	AP	1981/04/16	Control Supplement
018037	012	AP	1980/02/22	Labeling Revision
018037	010	AP	1980/06/18	Control Supplement
018037	008	AP	1980/05/30	Control Supplement
018037	007	AP	1980/08/07	Control Supplement
018037	006	AP	1980/05/28	Control Supplement
018037	005	AP	1979/08/02	Control Supplement
018037	003	AP	1980/06/28	Control Supplement
018037	002	AP	1979/06/14	Control Supplement
018037	001	AP	1980/02/25	Control Supplement
018037	000	AP	1979/02/02	Approval

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