TECHNETIUM TC 99M GENERATOR(TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR)

药品名称	TECHNETIUM TC 99M GENERATOR
申请号	017693	产品号	001
活性成分	TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR	市场状态	停止上市
剂型或给药途径	SOLUTION;INTRAVENOUS, ORAL	规格	830-16600mCi/GENERATOR
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	GE HEALTHCARE
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

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
017693	029	AP	2015/08/07	Labeling Revision
017693	027	AP	2015/01/05	Manufacturing Change or Addition
017693	026	AP	2014/10/14	Labeling Revision
017693	025	AP	2013/12/13	Manufacturing Change or Addition
017693	024	AP	1998/07/28	Manufacturing Change or Addition
017693	023	AP	1997/03/24	Manufacturing Change or Addition
017693	022	AP	1993/06/11	Manufacturing Change or Addition
017693	021	AP	1995/04/27	Manufacturing Change or Addition
017693	020	AP	1995/04/17	Manufacturing Change or Addition
017693	019	AP	1990/11/16	Control Supplement
017693	017	AP	1989/02/17	Control Supplement
017693	015	AP	1987/06/30	Manufacturing Change or Addition
017693	014	AP	1986/01/31	Manufacturing Change or Addition
017693	013	AP	1987/06/08	Labeling Revision
017693	011	AP	1988/06/01	Control Supplement
017693	010	AP	1984/01/10	Labeling Revision
017693	009	AP	1983/02/09	General Efficacy (MarkIV)
017693	008	AP	1982/06/07	Labeling Revision
017693	007	AP	1979/12/28	Manufacturing Change or Addition
017693	006	AP	1978/10/20	Manufacturing Change or Addition
017693	005	AP	1979/01/31	Labeling Revision
017693	003	AP	1978/02/13	Labeling Revision
017693	002	AP	1978/01/19	Manufacturing Change or Addition
017693	001	AP	1978/07/19	Control Supplement
017693	000	AP	1976/11/15	Approval