CORGARD(NADOLOL) - 美国FDA药品数据库

药品名称	CORGARD
申请号	018063	产品号	003
活性成分	NADOLOL	市场状态	停止上市
剂型或给药途径	TABLET;ORAL	规格	120MG
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	US WORLDMEDS LLC
化学类型	New molecular entity (NME)	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

与本品相关的市场独占权保护信息
独占权代码	失效日期
无
历史市场独占权保护信息
无

与药品注册相关的信息
申请号	修订号	审批结论	公开文档类型	文档创建时间	获取文档
018063	063	AP	Label	2013/07/15	下载
018063	063	AP	Letter	2013/07/16	下载
018063	062	AP	Letter	2011/06/07	下载
018063	062	AP	Label	2011/06/27	下载
018063	060	AP	Letter	2008/02/07	下载
018063	060	AP	Label	2008/02/14	下载

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
018063	063	AP	2013/07/15	Labeling Revision
018063	062	AP	2011/06/06	Labeling Revision
018063	060	AP	2008/02/04	Labeling Revision
018063	058	AP	2001/09/19	Manufacturing Change or Addition
018063	057	AP	1996/03/18	Control Supplement
018063	056	AP	1995/08/16	Manufacturing Change or Addition
018063	055	AP	1994/04/05	Control Supplement
018063	054	AP	1992/05/01	Formulation Revision
018063	053	AP	1992/05/20	Manufacturing Change or Addition
018063	052	AP	1991/11/08	Manufacturing Change or Addition
018063	051	AP	1991/05/03	Control Supplement
018063	050	AP	1991/03/29	Manufacturing Change or Addition
018063	049	AP	1990/11/07	Labeling Revision
018063	048	AP	1987/09/03	Package Change
018063	047	AP	1990/08/21	Control Supplement
018063	046	AP	1987/01/06	Package Change
018063	045	AP	1987/03/11	Expiration Date Change
018063	043	AP	1986/08/19	Control Supplement
018063	042	AP	1986/10/07	Control Supplement
018063	040	AP	1985/05/15	Labeling Revision
018063	039	AP	1984/10/24	Package Change
018063	038	AP	1984/08/06	Control Supplement
018063	037	AP	1984/05/16	Control Supplement
018063	036	AP	1984/05/15	Control Supplement
018063	035	AP	1986/10/28	New Dosage Regimen
018063	034	AP	1984/05/16	Expiration Date Change
018063	033	AP	1984/03/06	Package Change
018063	032	AP	1984/02/08	Package Change
018063	031	AP	1984/01/17	Control Supplement
018063	030	AP	1984/11/16	General Efficacy (MarkIV)
018063	029	AP	1983/11/01	Expiration Date Change
018063	028	AP	1983/10/14	Control Supplement
018063	027	AP	1983/07/21	Control Supplement
018063	026	AP	1983/03/29	Control Supplement
018063	024	AP	1983/03/29	Manufacturing Change or Addition
018063	023	AP	1982/11/18	Package Change
018063	022	AP	1982/09/22	Manufacturing Change or Addition
018063	021	AP	1982/10/01	Control Supplement
018063	019	AP	1982/06/02	Control Supplement
018063	018	AP	1982/04/01	Control Supplement
018063	017	AP	1982/03/02	Control Supplement
018063	016	AP	1981/10/15	Expiration Date Change
018063	015	AP	1981/08/28	Control Supplement
018063	014	AP	1981/07/24	Formulation Revision
018063	013	AP	1981/07/09	Formulation Revision
018063	012	AP	1981/04/02	Control Supplement
018063	011	AP	1981/08/28	Package Change
018063	010	AP	1981/01/27	Package Change
018063	009	AP	1981/03/17	Control Supplement
018063	008	AP	1980/12/30	Labeling Revision
018063	005	AP	1980/10/22	Control Supplement
018063	004	AP	1981/01/27	Formulation Revision
018063	003	AP	1980/08/14	Manufacturing Change or Addition
018063	002	AP	1980/02/11	Labeling Revision
018063	001	AP	1980/02/11	Labeling Revision
018063	000	AP	1979/12/10	Approval

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