CATAPRES(CLONIDINE HYDROCHLORIDE) - 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
017407	038	AP	2015/05/21	Manufacturing Change or Addition
017407	037	AP	2012/05/31	Labeling Revision
017407	036	AP	2010/04/07	Labeling Revision
017407	034	AP	2009/11/09	Labeling Revision
017407	033	AP	2010/01/05	Labeling Revision
017407	031	AP	1999/04/13	Manufacturing Change or Addition
017407	030	AP	1998/04/30	Control Supplement
017407	029	AP	1997/11/03	Control Supplement
017407	028	AP	1996/08/02	Labeling Revision
017407	027	AP	1996/08/02	Labeling Revision
017407	026	AP	1988/06/20	Labeling Revision
017407	025	AP	1987/03/26	Labeling Revision
017407	024	AP	1987/09/02	Manufacturing Change or Addition
017407	023	AP	1986/04/11	Labeling Revision
017407	022	AP	1985/10/02	Labeling Revision
017407	021	AP	1985/03/06	Control Supplement
017407	020	AP	1984/04/06	Formulation Revision
017407	019	AP	1987/09/08	Practioner Draft Labeling
017407	018	AP	1982/11/03	Manufacturing Change or Addition
017407	017	AP	1981/08/05	Package Change
017407	016	AP	1981/04/06	Package Change
017407	015	AP	1981/02/20	Package Change
017407	014	AP	1981/02/20	Package Change
017407	013	AP	1980/09/12	Package Change
017407	012	AP	1980/09/16	Expiration Date Change
017407	011	AP	1980/02/26	Package Change
017407	010	AP	1980/12/10	Package Change
017407	009	AP	1978/11/27	Package Change
017407	008	AP	1979/09/20	General Efficacy (MarkIV)
017407	006	AP	1981/02/05	Package Change
017407	005	AP	1976/12/10	Package Change
017407	004	AP	1977/01/17	Package Change
017407	003	AP	1976/10/27	Formulation Revision
017407	002	AP	1976/07/26	Package Change
017407	001	AP	1976/06/08	Package Change
017407	000	AP	1974/09/03	Approval