DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 20MEQ (K) IN PLASTIC CONTAINER(DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)

药品名称	DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 20MEQ (K) IN PLASTIC CONTAINER
申请号	018008	产品号	001
活性成分	DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	市场状态	停止上市
剂型或给药途径	INJECTABLE;INJECTION	规格	5GM/100ML;300MG/100ML;450MG/100ML
治疗等效代码		参比药物	否
批准日期	Approved Prior to Jan 1, 1982	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
018008	070	AP	Label	2013/09/11	下载
018008	070	AP	Letter	2013/09/12	下载
018008	066	AP	Label	2007/04/25	下载
018008	066	AP	Letter	2007/05/01	下载
018008	065	AP	Label	2005/08/31	下载
018008	065	AP	Letter	2005/08/31	下载
018008	063	AP	Letter	2004/06/07	下载
018008	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
018008	071	AP	2014/09/26	Manufacturing Change or Addition
018008	070	AP	2013/09/10	Labeling Revision
018008	066	AP	2007/04/20	Labeling Revision
018008	065	AP	2005/08/26	Package Change
018008	063	AP	2004/06/02	Labeling Revision
018008	060	AP	2001/08/14	Manufacturing Change or Addition
018008	059	AP	2003/04/14	Labeling Revision
018008	058	AP	1999/11/24	Manufacturing Change or Addition
018008	057	AP	1997/04/29	Package Change
018008	056	AP	1994/02/18	Control Supplement
018008	055	AP	1994/09/30	Control Supplement
018008	054	AP	1993/04/22	Labeling Revision
018008	053	AP	1991/12/11	Control Supplement
018008	051	AP	1991/04/29	Control Supplement
018008	050	AP	1991/03/26	Control Supplement
018008	049	AP	1991/02/15	Control Supplement
018008	048	AP	1989/07/26	Control Supplement
018008	047	AP	1987/07/25	Package Change
018008	046	AP	1987/05/28	Control Supplement
018008	044	AP	1986/02/27	Package Change
018008	043	AP	1985/04/15	Control Supplement
018008	042	AP	1985/07/03	Labeling Revision
018008	041	AP	1985/06/13	Control Supplement
018008	040	AP	1984/10/23	Control Supplement
018008	039	AP	1984/02/28	Control Supplement
018008	037	AP	1985/08/28	Control Supplement
018008	036	AP	1985/08/28	Control Supplement
018008	035	AP	1984/03/16	Control Supplement
018008	034	AP	1985/01/24	Control Supplement
018008	032	AP	1982/05/25	Labeling Revision
018008	031	AP	1982/04/28	Labeling Revision
018008	029	AP	1983/07/11	Practioner Draft Labeling
018008	028	AP	1981/11/20	Control Supplement
018008	026	AP	1982/06/03	Control Supplement
018008	025	AP	1981/11/09	Control Supplement
018008	024	AP	1982/04/16	Control Supplement
018008	023	AP	1981/08/26	Labeling Revision
018008	022	AP	1981/12/21	Control Supplement
018008	020	AP	1981/06/29	Control Supplement
018008	019	AP	1981/05/29	Control Supplement
018008	018	AP	1981/01/21	Control Supplement
018008	017	AP	1980/07/31	Control Supplement
018008	014	AP	1980/08/06	Control Supplement
018008	013	AP	1981/04/16	Control Supplement
018008	012	AP	1980/02/22	Labeling Revision
018008	010	AP	1980/06/18	Control Supplement
018008	008	AP	1980/05/28	Control Supplement
018008	007	AP	1980/05/30	Control Supplement
018008	006	AP	1980/08/07	Control Supplement
018008	005	AP	1979/08/02	Control Supplement
018008	003	AP	1980/06/28	Control Supplement
018008	002	AP	1979/06/14	Control Supplement
018008	001	AP	1980/02/25	Control Supplement
018008	000	AP	1979/02/02	Approval

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