药品名称COMBIPRES
申请号017503产品号001
活性成分CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格15MG;0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构BOEHRINGER INGELHEIM PHARMACEUTICALS INC
化学类型审评分类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
历史专利信息
与本品相关的市场独占权保护信息
独占权代码失效日期
历史市场独占权保护信息
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
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
017503028AP1999/09/15Manufacturing Change or Addition
017503027AP1991/04/08Control Supplement
017503026AP1991/02/20Labeling Revision
017503025AP1987/08/07Control Supplement
017503024AP1987/03/26Labeling Revision
017503023AP1986/04/10Labeling Revision
017503022AP1985/10/02Labeling Revision
017503021AP1984/12/18Control Supplement
017503020AP1985/02/25Control Supplement
017503019AP1984/11/19Control Supplement
017503018AP1984/08/01Control Supplement
017503017AP1984/04/10Labeling Revision
017503016AP1983/03/09Manufacturing Change or Addition
017503015AP1981/07/31Package Change
017503014AP1981/04/09Package Change
017503013AP1980/11/28Package Change
017503012AP1981/01/15Package Change
017503011AP1980/11/28Package Change
017503010AP1980/11/28Formulation Revision
017503009AP1980/02/26Package Change
017503008AP1980/02/26Package Change
017503007AP1979/01/31Package Change
017503005AP1981/02/05Package Change
017503004AP1976/12/10Package Change
017503003AP1977/01/17Package Change
017503002AP1976/07/09Package Change
017503001AP1976/06/08Package Change
017503000AP1974/09/03Approval