RINGER'S IN PLASTIC CONTAINER(CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)

药品名称	RINGER'S IN PLASTIC CONTAINER
申请号	016693	产品号	001
活性成分	CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	市场状态	处方药
剂型或给药途径	INJECTABLE;INJECTION	规格	33MG/100ML;30MG/100ML;860MG/100ML
治疗等效代码	AP	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
016693	098	AP	Letter	2016/04/28	下载
016693	098	AP	Label	2016/05/05	下载
016693	096	AP	Letter	2013/09/13	下载
016693	096	AP	Label	2013/09/17	下载
016693	084	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
016693	098	AP	2016/04/27	Labeling Revision
016693	097	AP	2014/09/30	Manufacturing Change or Addition
016693	096	AP	2013/09/11	Labeling Revision
016693	087	AP	2001/08/14	Manufacturing Change or Addition
016693	086	AP	2000/11/02	Labeling Revision
016693	085	AP	1999/11/24	Manufacturing Change or Addition
016693	084	AP	2002/04/03	Labeling Revision
016693	083	AP	1997/04/29	Package Change
016693	082	AP	1994/02/18	Control Supplement
016693	081	AP	1994/09/30	Control Supplement
016693	079	AP	1991/01/22	Control Supplement
016693	078	AP	1991/04/29	Control Supplement
016693	077	AP	1991/03/26	Control Supplement
016693	076	AP	1991/02/15	Control Supplement
016693	075	AP	1989/07/26	Control Supplement
016693	074	AP	1987/07/25	Package Change
016693	073	AP	1987/05/28	Control Supplement
016693	071	AP	1986/02/27	Package Change
016693	070	AP	1985/04/15	Control Supplement
016693	069	AP	1985/07/03	Labeling Revision
016693	068	AP	1985/06/13	Control Supplement
016693	067	AP	1984/09/22	Control Supplement
016693	066	AP	1984/02/28	Control Supplement
016693	064	AP	1985/08/28	Control Supplement
016693	063	AP	1985/08/28	Control Supplement
016693	062	AP	1984/03/16	Control Supplement
016693	061	AP	1985/01/24	Control Supplement
016693	059	AP	1982/02/16	Control Supplement
016693	058	AP	1983/07/11	Practioner Draft Labeling
016693	057	AP	1981/11/20	Control Supplement
016693	055	AP	1982/06/03	Control Supplement
016693	054	AP	1981/11/09	Control Supplement
016693	053	AP	1982/04/16	Control Supplement
016693	052	AP	1981/08/26	Labeling Revision
016693	051	AP	1981/12/21	Control Supplement
016693	049	AP	1981/06/29	Control Supplement
016693	048	AP	1981/01/21	Control Supplement
016693	047	AP	1980/07/31	Control Supplement
016693	046	AP	1981/04/16	Control Supplement
016693	044	AP	1980/06/18	Control Supplement
016693	043	AP	1980/05/30	Control Supplement
016693	042	AP	1980/08/07	Control Supplement
016693	040	AP	1980/06/28	Control Supplement
016693	039	AP	1979/08/02	Control Supplement
016693	037	AP	1978/10/20	Control Supplement
016693	036	AP	1978/08/07	Control Supplement
016693	035	AP	1978/08/02	Control Supplement
016693	034	AP	1978/04/25	Labeling Revision
016693	033	AP	1978/03/22	Control Supplement
016693	032	AP	1980/02/25	Control Supplement
016693	031	AP	1978/06/20	Control Supplement
016693	030	AP	1978/03/24	Control Supplement
016693	029	AP	1978/02/21	Control Supplement
016693	028	AP	1978/02/28	Control Supplement
016693	027	AP	1977/12/14	Control Supplement
016693	026	AP	1977/06/06	Control Supplement
016693	025	AP	1977/02/07	Package Change
016693	024	AP	1976/07/13	Final Printed Labeling - MarkIV
016693	023	AP	1976/06/17	Control Supplement
016693	021	AP	1976/01/02	Labeling Revision
016693	020	AP	1976/07/01	Control Supplement
016693	019	AP	1976/01/05	Control Supplement
016693	018	AP	1976/12/21	Labeling Revision
016693	017	AP	1975/09/23	Control Supplement
016693	016	AP	1976/05/11	Labeling Revision
016693	015	AP	1975/09/17	Control Supplement
016693	014	AP	1975/06/16	Control Supplement
016693	012	AP	1975/07/10	Control Supplement
016693	000	AP	1971/03/22	Approval

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