药品名称ALDOCLOR-250
申请号016016产品号002
活性成分CHLOROTHIAZIDE; METHYLDOPA市场状态停止上市
剂型或给药途径TABLET;ORAL规格250MG;250MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构MERCK AND CO INC
化学类型New combination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
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
016016070AP1999/08/22Labeling Revision
016016069AP1997/08/05Labeling Revision
016016068AP1997/05/23Control Supplement
016016067AP1994/09/26Manufacturing Change or Addition
016016066AP1994/12/16Labeling Revision
016016065AP1994/06/30Labeling Revision
016016064AP1992/09/17Labeling Revision
016016063AP1990/09/13Labeling Revision
016016062AP1988/09/06Manufacturing Change or Addition
016016061AP1992/09/03Labeling Revision
016016060AP1988/04/21Labeling Revision
016016059AP1987/08/26Labeling Revision
016016058AP1988/08/15Control Supplement
016016057AP1986/06/02Labeling Revision
016016056AP1986/01/14Labeling Revision
016016055AP1984/09/24Labeling Revision
016016054AP1984/04/03Labeling Revision
016016053AP1983/12/23Formulation Revision
016016052AP1982/04/21Labeling Revision
016016051AP1987/05/08Practioner Draft Labeling
016016050AP1981/09/23Labeling Revision
016016049AP1981/06/17Package Change
016016048AP1981/04/27Labeling Revision
016016047AP1981/04/09Control Supplement
016016046AP1981/01/23Formulation Revision
016016045AP1981/01/13Labeling Revision
016016044AP1980/11/14Package Change
016016043AP1981/04/09Formulation Revision
016016042AP1979/11/29Labeling Revision
016016041AP1979/07/03Labeling Revision
016016040AP1979/09/18Labeling Revision
016016039AP1979/03/09Control Supplement
016016038AP1978/11/07Control Supplement
016016037AP1978/08/29Control Supplement
016016036AP1979/06/18Formulation Revision
016016035AP1979/06/18Control Supplement
016016034AP1978/09/12Labeling Revision
016016033AP1978/02/15Package Change
016016032AP1978/09/12Labeling Revision
016016031AP1976/11/09Control Supplement
016016030AP1976/02/19Labeling Revision
016016029AP1975/06/06Control Supplement
016016000AP1968/03/20Approval