PRALIDOXIME CHLORIDE(PRALIDOXIME CHLORIDE)

药品名称	PRALIDOXIME CHLORIDE
申请号	018986	产品号	001
活性成分	PRALIDOXIME CHLORIDE	市场状态	处方药
剂型或给药途径	INJECTABLE;INJECTION	规格	300MG/ML
治疗等效代码		参比药物	是
批准日期	1983/04/26	申请机构	MERIDIAN MEDICAL TECHNOLOGIES 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

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
018986	045	AP	2015/01/05	Manufacturing Change or Addition
018986	044	AP	2014/08/21	Manufacturing Change or Addition
018986	043	AP	2013/12/31	Manufacturing Change or Addition
018986	022	AP	2002/10/24	Control Supplement
018986	021	AP	2002/06/28	Manufacturing Change or Addition
018986	020	AP	2002/03/01	Manufacturing Change or Addition
018986	019	AP	2002/02/25	Control Supplement
018986	018	AP	2002/02/15	Manufacturing Change or Addition
018986	017	AP	2001/01/23	Package Change
018986	016	AP	2000/11/02	Control Supplement
018986	015	AP	2001/11/28	Manufacturing Change or Addition
018986	014	AP	2000/01/27	Manufacturing Change or Addition
018986	013	AP	1999/10/28	Manufacturing Change or Addition
018986	012	AP	1999/12/10	Manufacturing Change or Addition
018986	011	AP	1998/10/08	Manufacturing Change or Addition
018986	010	AP	1998/04/21	Labeling Revision
018986	009	AP	1997/03/06	Manufacturing Change or Addition
018986	008	AP	1996/08/23	Manufacturing Change or Addition
018986	007	AP	1991/03/18	Labeling Revision
018986	005	AP	1986/07/31	Labeling Revision
018986	004	AP	1986/03/21	Control Supplement
018986	003	AP	1985/05/14	Control Supplement
018986	002	AP	1986/02/26	Labeling Revision
018986	001	AP	1985/02/06	Expiration Date Change
018986	000	AP	1983/04/26	Approval