SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINER(SODIUM LACTATE)

药品名称	SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINER
申请号	016692	产品号	001
活性成分	SODIUM LACTATE	市场状态	停止上市
剂型或给药途径	INJECTABLE;INJECTION	规格	1.87GM/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
016692	095	AP	Letter	2011/10/24	下载
016692	095	AP	Label	2011/11/04	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
016692	099	AP	2015/01/12	Manufacturing Change or Addition
016692	098	AP	2013/04/26	Manufacturing Change or Addition
016692	095	AP	2011/10/19	Labeling Revision
016692	088	AP	2001/08/14	Manufacturing Change or Addition
016692	087	AP	2000/11/02	Labeling Revision
016692	086	AP	1999/11/24	Manufacturing Change or Addition
016692	085	AP	2000/11/29	Labeling Revision
016692	084	AP	1997/04/29	Package Change
016692	083	AP	1994/02/18	Control Supplement
016692	082	AP	1994/09/30	Control Supplement
016692	080	AP	1991/04/26	Control Supplement
016692	079	AP	1991/04/29	Control Supplement
016692	078	AP	1991/03/26	Control Supplement
016692	077	AP	1991/02/15	Control Supplement
016692	076	AP	1989/07/26	Control Supplement
016692	075	AP	1987/07/25	Package Change
016692	074	AP	1987/05/28	Control Supplement
016692	072	AP	1986/02/27	Package Change
016692	071	AP	1985/04/15	Control Supplement
016692	068	AP	1985/04/17	Labeling Revision
016692	067	AP	1985/06/13	Control Supplement
016692	066	AP	1984/09/22	Control Supplement
016692	065	AP	1984/02/28	Control Supplement
016692	063	AP	1985/08/28	Control Supplement
016692	062	AP	1985/08/28	Control Supplement
016692	061	AP	1984/03/16	Control Supplement
016692	060	AP	1985/01/24	Control Supplement
016692	058	AP	1982/02/16	Control Supplement
016692	057	AP	1983/07/11	Practioner Draft Labeling
016692	056	AP	1981/11/20	Control Supplement
016692	054	AP	1982/06/03	Control Supplement
016692	053	AP	1982/04/16	Control Supplement
016692	052	AP	1981/08/26	Labeling Revision
016692	051	AP	1981/12/21	Control Supplement
016692	049	AP	1981/06/29	Control Supplement
016692	048	AP	1981/01/21	Control Supplement
016692	046	AP	1980/07/31	Control Supplement
016692	045	AP	1981/04/16	Control Supplement
016692	042	AP	1980/05/30	Control Supplement
016692	041	AP	1980/08/07	Control Supplement
016692	039	AP	1980/06/28	Control Supplement
016692	038	AP	1979/08/02	Control Supplement
016692	036	AP	1978/10/20	Control Supplement
016692	035	AP	1978/08/07	Control Supplement
016692	034	AP	1978/08/02	Control Supplement
016692	033	AP	1978/04/25	Labeling Revision
016692	032	AP	1978/03/22	Control Supplement
016692	031	AP	1980/02/25	Control Supplement
016692	030	AP	1978/06/20	Control Supplement
016692	029	AP	1978/03/24	Control Supplement
016692	028	AP	1978/02/28	Control Supplement
016692	027	AP	1977/12/14	Control Supplement
016692	026	AP	1977/06/06	Control Supplement
016692	025	AP	1977/02/07	Package Change
016692	024	AP	1976/07/13	Final Printed Labeling - MarkIV
016692	023	AP	1976/06/17	Control Supplement
016692	021	AP	1976/07/01	Labeling Revision
016692	019	AP	1976/01/05	Control Supplement
016692	018	AP	1976/10/18	Labeling Revision
016692	017	AP	1975/09/23	Control Supplement
016692	016	AP	1976/05/11	Labeling Revision
016692	015	AP	1975/09/17	Control Supplement
016692	014	AP	1975/09/25	Control Supplement
016692	012	AP	1975/07/10	Control Supplement
016692	000	AP	1971/03/22	Approval

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