CELEXA(CITALOPRAM HYDROBROMIDE) - 美国FDA药品数据库

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
020822	046	AP	2014/07/08	Labeling Revision
020822	045	AP	2014/04/16	Labeling Revision
020822	044	AP	2013/06/17	Manufacturing Change or Addition
020822	043	AP	2012/12/03	Labeling Revision
020822	042	AP	2012/03/27	Labeling Revision
020822	040	AP	2011/08/12	Labeling Revision
020822	038	AP	2011/08/12	Labeling Revision
020822	037	AP	2009/01/30	Labeling Revision
020822	035	AP	2008/09/17	Labeling Revision
020822	034	AP	2007/08/02	Labeling Revision
020822	029	AP	2005/02/18	Labeling Revision
020822	027	AP	2004/05/20	Labeling Revision
020822	023	AP	2004/04/08	Labeling Revision
020822	019	AP	2002/11/19	Labeling Revision
020822	015	AP	2002/05/30	Manufacturing Change or Addition
020822	014	AP	2001/07/10	Manufacturing Change or Addition
020822	013	AP	2001/05/17	Manufacturing Change or Addition
020822	012	AP	2000/11/22	Manufacturing Change or Addition
020822	011	AP	2001/06/27	Labeling Revision
020822	010	AP	2000/06/27	Manufacturing Change or Addition
020822	008	AP	2000/04/27	Manufacturing Change or Addition
020822	007	AP	2000/07/13	Control Supplement
020822	006	AP	1999/12/07	Control Supplement
020822	005	AP	1999/12/07	Control Supplement
020822	003	AP	1999/10/21	Package Change
020822	002	AP	1999/08/13	Manufacturing Change or Addition
020822	001	AP	1999/10/19	Control Supplement
020822	000	AP	1998/07/17	Approval