DEXTROSE 30% IN PLASTIC CONTAINER(DEXTROSE)

药品名称	DEXTROSE 30% IN PLASTIC CONTAINER
申请号	017521	产品号	003
活性成分	DEXTROSE	市场状态	处方药
剂型或给药途径	INJECTABLE;INJECTION	规格	30GM/100ML
治疗等效代码	AP	参比药物	是
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
017521	068	AP	Letter	2014/12/24	下载
017521	068	AP	Label	2015/01/09	下载
017521	063	AP	Letter	2003/07/31	下载
017521	063	AP	Review	2007/09/24	下载
017521	062	AP	Letter	2003/07/31	下载
017521	062	AP	Review	2007/09/24	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
017521	072	AP	2016/03/23	Manufacturing Change or Addition
017521	071	AP	2016/01/15	Manufacturing Change or Addition
017521	070	AP	2015/02/03	Manufacturing Change or Addition
017521	068	AP	2014/12/22	Labeling Revision
017521	064	AP	2001/08/14	Manufacturing Change or Addition
017521	063	AP	2002/11/14	Labeling Revision
017521	062	AP	2002/11/14	Labeling Revision
017521	061	AP	2000/12/07	Efficacy Supplement with Clinical Data to Support
017521	060	AP	1999/11/24	Manufacturing Change or Addition
017521	059	AP	1999/05/25	Manufacturing Change or Addition
017521	058	AP	1998/06/22	Control Supplement
017521	057	AP	1997/04/29	Package Change
017521	056	AP	1994/02/18	Control Supplement
017521	055	AP	1994/09/30	Control Supplement
017521	052	AP	1993/07/13	Manufacturing Change or Addition
017521	051	AP	1991/03/26	Control Supplement
017521	050	AP	1995/01/05	Labeling Revision
017521	049	AP	1995/01/05	Control Supplement
017521	048	AP	1990/05/18	Control Supplement
017521	047	AP	1991/02/15	Control Supplement
017521	042	AP	1989/07/26	Control Supplement
017521	041	AP	1989/01/12	Control Supplement
017521	039	AP	1987/12/09	Package Change
017521	038	AP	1985/04/23	Labeling Revision
017521	037	AP	1985/04/15	Control Supplement
017521	036	AP	1984/09/21	Control Supplement
017521	035	AP	1985/06/13	Control Supplement
017521	034	AP	1984/09/22	Control Supplement
017521	033	AP	1984/08/24	Practioner Draft Labeling
017521	032	AP	1984/02/28	Control Supplement
017521	028	AP	1984/03/16	Control Supplement
017521	027	AP	1985/01/24	Control Supplement
017521	025	AP	1982/02/16	Control Supplement
017521	024	AP	1981/11/20	Control Supplement
017521	022	AP	1982/06/03	Control Supplement
017521	021	AP	1981/11/09	Control Supplement
017521	018	AP	1982/04/16	Control Supplement
017521	017	AP	1981/08/26	Labeling Revision
017521	016	AP	1981/12/21	Control Supplement
017521	015	AP	1982/03/26	Labeling Revision
017521	014	AP	1982/03/26	Control Supplement
017521	012	AP	1981/06/29	Control Supplement
017521	011	AP	1981/01/21	Control Supplement
017521	010	AP	1980/09/09	Labeling Revision
017521	009	AP	1980/09/09	Control Supplement
017521	008	AP	1980/07/31	Control Supplement
017521	007	AP	1980/08/06	Control Supplement
017521	006	AP	1981/04/16	Control Supplement
017521	005	AP	1980/02/11	Control Supplement
017521	004	AP	1980/06/18	Control Supplement
017521	003	AP	1980/05/30	Control Supplement
017521	002	AP	1980/07/18	Labeling Revision
017521	001	AP	1980/07/18	Control Supplement
017521	000	AP	1979/08/28	Approval

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