MS CONTIN(MORPHINE SULFATE) - 美国FDA药品数据库

药品名称	MS CONTIN
申请号	019516	产品号	005
活性成分	MORPHINE SULFATE	市场状态	处方药
剂型或给药途径	TABLET, EXTENDED RELEASE;ORAL	规格	200MG
治疗等效代码	AB	参比药物	否
批准日期	1993/11/08	申请机构	PURDUE PHARMA LP
化学类型	New dosage form	审评分类	Priority 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
019516	050	AP	2016/09/30	Supplement
019516	048	AP	2016/09/21	Manufacturing Change or Addition
019516	047	AP	2016/04/20	Supplement
019516	046	AP	2015/06/26	Supplement
019516	044	AP	2014/08/19	Supplement
019516	043	AP	2014/10/22	Labeling Revision
019516	042	AP	2014/04/16	Labeling Revision
019516	040	AP	2014/06/02	Manufacturing Change or Addition
019516	038	AP	2013/04/15	Labeling Revision
019516	037	AP	2012/07/09	Labeling Revision
019516	036	AP	2012/07/09	Labeling Revision
019516	034	AP	2010/05/11	Labeling Revision
019516	030	AP	2007/05/11	Supplement
019516	021	AP	2003/08/06	Labeling Revision
019516	019	AP	2003/02/21	Package Change
019516	016	AP	2001/12/18	Labeling Revision
019516	015	AP	2001/02/12	Labeling Revision
019516	014	AP	2000/05/02	Manufacturing Change or Addition
019516	013	AP	2000/06/27	Manufacturing Change or Addition
019516	012	AP	2000/05/02	Manufacturing Change or Addition
019516	011	AP	2000/05/02	Manufacturing Change or Addition
019516	010	AP	2000/05/02	Manufacturing Change or Addition
019516	009	AP	2000/05/02	Manufacturing Change or Addition
019516	008	AP	2000/05/12	Control Supplement
019516	007	AP	1997/04/29	Manufacturing Change or Addition
019516	006	AP	1990/04/12	Formulation Revision
019516	005	AP	1988/05/02	Control Supplement
019516	004	AP	1993/11/08	Control Supplement
019516	003	AP	1990/01/16	Control Supplement
019516	002	AP	1989/09/12	Control Supplement
019516	001	AP	1988/04/08	Control Supplement
019516	000	AP	1987/05/29	Approval