DEXTROSE 5% AND SODIUM CHLORIDE 0.225% IN PLASTIC CONTAINER(DEXTROSE; SODIUM CHLORIDE)

药品名称	DEXTROSE 5% AND SODIUM CHLORIDE 0.225% IN PLASTIC CONTAINER
申请号	017606	产品号	001
活性成分	DEXTROSE; SODIUM CHLORIDE	市场状态	处方药
剂型或给药途径	INJECTABLE;INJECTION	规格	5GM/100ML;225MG/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	HOSPIRA INC
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
无

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
017606	141	AP	2013/09/05	Manufacturing Change or Addition
017606	116	AP	2000/03/21	Labeling Revision
017606	115	AP	1998/10/29	Control Supplement
017606	114	AP	1997/06/11	Manufacturing Change or Addition
017606	113	AP	1997/08/20	Labeling Revision
017606	112	AP	1997/03/28	Control Supplement
017606	111	AP	1996/08/06	Control Supplement
017606	110	AP	1996/03/04	Control Supplement
017606	109	AP	1995/08/18	Manufacturing Change or Addition
017606	108	AP	1996/08/29	Control Supplement
017606	107	AP	1996/08/27	Control Supplement
017606	105	AP	1995/08/14	Control Supplement
017606	102	AP	1991/08/30	Package Change
017606	101	AP	1992/01/28	Package Change
017606	100	AP	1991/09/10	Control Supplement
017606	098	AP	1990/01/11	Manufacturing Change or Addition
017606	097	AP	1990/02/22	Manufacturing Change or Addition
017606	094	AP	1987/07/30	Control Supplement
017606	093	AP	1986/11/26	Control Supplement
017606	092	AP	1986/08/08	Control Supplement
017606	091	AP	1985/06/10	Control Supplement
017606	090	AP	1985/09/30	Expiration Date Change
017606	089	AP	1986/01/31	Control Supplement
017606	086	AP	1985/08/27	Expiration Date Change
017606	085	AP	1985/10/26	Labeling Revision
017606	084	AP	1985/05/03	Control Supplement
017606	083	AP	1985/10/26	Control Supplement
017606	080	AP	1984/10/22	Control Supplement
017606	079	AP	1985/09/26	Package Change
017606	077	AP	1985/11/29	Labeling Revision
017606	076	AP	1985/11/29	Control Supplement
017606	075	AP	1985/10/29	Package Change
017606	074	AP	1984/11/28	Control Supplement
017606	073	AP	1988/08/31	Control Supplement
017606	072	AP	1984/04/09	Control Supplement
017606	071	AP	1984/06/14	Expiration Date Change
017606	070	AP	1984/10/17	Control Supplement
017606	069	AP	1984/03/21	Control Supplement
017606	068	AP	1983/08/31	Control Supplement
017606	067	AP	1983/12/08	Control Supplement
017606	066	AP	1984/02/17	Control Supplement
017606	065	AP	1983/06/06	Manufacturing Change or Addition
017606	064	AP	1984/10/10	Labeling Revision
017606	063	AP	1984/10/10	Package Change
017606	062	AP	1982/07/26	Control Supplement
017606	061	AP	1984/03/01	Control Supplement
017606	060	AP	1983/02/15	Manufacturing Change or Addition
017606	059	AP	1982/07/08	Control Supplement
017606	058	AP	1982/02/01	Control Supplement
017606	057	AP	1982/02/05	Control Supplement
017606	056	AP	1982/01/08	Control Supplement
017606	055	AP	1982/06/09	Control Supplement
017606	054	AP	1981/10/07	Control Supplement
017606	053	AP	1981/10/21	Labeling Revision
017606	052	AP	1981/10/21	Control Supplement
017606	051	AP	1981/03/02	Labeling Revision
017606	050	AP	1982/08/31	Practioner Draft Labeling
017606	049	AP	1981/03/02	Labeling Revision
017606	048	AP	1981/03/02	Control Supplement
017606	047	AP	1981/01/07	Control Supplement
017606	046	AP	1980/09/15	Control Supplement
017606	045	AP	1980/06/10	Control Supplement
017606	044	AP	1980/02/12	Control Supplement
017606	043	AP	1980/04/08	Labeling Revision
017606	042	AP	1979/10/10	Control Supplement
017606	041	AP	1979/11/29	Control Supplement
017606	040	AP	1980/01/22	Control Supplement
017606	039	AP	1979/11/27	Control Supplement
017606	038	AP	1979/12/03	Control Supplement
017606	037	AP	1979/12/03	Control Supplement
017606	036	AP	1979/07/17	Labeling Revision
017606	035	AP	1979/01/05	Control Supplement
017606	034	AP	1979/02/01	Supplement
017606	033	AP	1978/11/07	Labeling Revision
017606	032	AP	1978/11/08	Control Supplement
017606	031	AP	1978/11/22	Control Supplement
017606	030	AP	1978/10/11	Control Supplement
017606	029	AP	1978/11/22	Control Supplement
017606	028	AP	1979/02/06	Control Supplement
017606	027	AP	1978/08/02	Control Supplement
017606	026	AP	1978/08/15	Control Supplement
017606	025	AP	1978/05/08	Control Supplement
017606	023	AP	1978/06/26	Control Supplement
017606	021	AP	1978/02/08	Labeling Revision
017606	020	AP	1978/03/30	Control Supplement
017606	019	AP	1978/06/14	Formulation Revision
017606	018	AP	1978/10/10	Labeling Revision
017606	017	AP	1978/10/10	Control Supplement
017606	016	AP	1978/02/13	Manufacturing Change or Addition
017606	015	AP	1977/09/28	Labeling Revision
017606	014	AP	1978/04/11	Control Supplement
017606	011	AP	1978/01/23	Control Supplement
017606	010	AP	1977/05/20	Control Supplement
017606	009	AP	1977/05/09	Control Supplement
017606	008	AP	1976/12/03	Labeling Revision
017606	007	AP	1978/06/14	Control Supplement
017606	006	AP	1977/04/29	Manufacturing Change or Addition
017606	005	AP	1976/11/08	Package Change
017606	004	AP	1975/10/22	Labeling Revision
017606	003	AP	1975/11/20	Control Supplement
017606	002	AP	1975/11/03	Control Supplement
017606	001	AP	1975/10/15	Control Supplement
017606	000	AP	1975/08/13	Approval

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