药品名称TIMENTIN
申请号050590产品号003
活性成分CLAVULANATE POTASSIUM; TICARCILLIN DISODIUM市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格EQ 1GM BASE/VIAL;EQ 30GM BASE/VIAL
治疗等效代码参比药物
批准日期1987/08/18申请机构GLAXOSMITHKLINE
化学类型New combination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
050590069APLetter2014/06/17下载
050590069APLabel2014/06/17下载
050590067APLetter2013/10/01下载
050590067APLabel2013/10/01下载
050590062APLabel2012/10/05下载
050590062APLetter2012/10/09下载
050590061APLetter2011/06/13下载
050590061APLabel2011/06/14下载
050590060APLabel2011/06/14下载
050590060APLetter2011/06/13下载
050590059APLetter2010/12/28下载
050590059APLabel2010/12/26下载
050590058APLetter2010/12/28下载
050590058APLabel2010/12/26下载
050590057APLetter2008/04/22下载
050590057APLabel2008/06/05下载
050590055APLetter2008/12/19下载
050590054APLabel2007/03/16下载
050590054APLetter2007/03/23下载
050590052APLetter2004/12/02下载
050590040APLetter2002/03/18下载
050590027APLetter2002/05/17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
050590069AP2014/06/12Labeling Revision
050590068AP2014/02/12Manufacturing Change or Addition
050590067AP2013/09/27Labeling Revision
050590066AP2013/07/19Manufacturing Change or Addition
050590065AP2013/03/20Manufacturing Change or Addition
050590062AP2012/10/04Labeling Revision
050590061AP2011/06/09Labeling Revision
050590060AP2011/06/09Labeling Revision
050590059AP2010/12/20Labeling Revision
050590058AP2010/12/20Labeling Revision
050590057AP2008/04/17Labeling Revision
050590055AP2008/05/08Labeling Revision
050590054AP2007/03/15Labeling Revision
050590052AP2004/11/19Labeling Revision
050590048AP2003/01/03Control Supplement
050590047AP2002/10/17Control Supplement
050590044AP2002/02/08Manufacturing Change or Addition
050590043AP2001/08/16Control Supplement
050590042AP2001/08/02Control Supplement
050590041AP2001/08/02Control Supplement
050590040AP2002/03/18Labeling Revision
050590037AP1999/11/19Control Supplement
050590036AP1999/09/23Control Supplement
050590035AP1999/02/01Control Supplement
050590034AP1998/02/05Manufacturing Change or Addition
050590033AP1997/08/29Package Change
050590032AP1999/07/07Control Supplement
050590031AP1997/06/17Manufacturing Change or Addition
050590030AP1997/12/11Patient Population Altered
050590029AP1996/02/27Labeling Revision
050590028AP1995/04/18Control Supplement
050590027AP2002/05/17Labeling Revision
050590026AP1994/09/16Control Supplement
050590025AP1996/01/19Labeling Revision
050590024AP1993/06/08Manufacturing Change or Addition
050590023AP1993/06/08Control Supplement
050590022AP1993/01/07Labeling Revision
050590021AP1987/12/01Labeling Revision
050590020AP1992/03/26Labeling Revision
050590019AP1992/03/26Labeling Revision
050590018AP1992/01/02Control Supplement
050590017AP1990/02/26Control Supplement
050590016AP1991/12/17New or Modified Indication
050590015AP1989/04/20Control Supplement
050590014AP1989/04/20Control Supplement
050590013AP1988/08/24Control Supplement
050590012AP1988/05/16Labeling Revision
050590011AP1987/08/18Labeling Revision
050590010AP1987/10/23New or Modified Indication
050590009AP1986/02/14Control Supplement
050590006AP1985/11/26Control Supplement
050590005AP1985/11/26Control Supplement
050590004AP1985/08/12Control Supplement
050590003AP1985/04/18Labeling Revision
050590002AP1985/04/19Manufacturing Change or Addition
050590001AP1985/05/13Control Supplement
050590000AP1985/04/01Approval