药品名称TEGRETOL
申请号018927产品号001
活性成分CARBAMAZEPINE市场状态处方药
剂型或给药途径SUSPENSION;ORAL规格100MG/5ML
治疗等效代码AB参比药物
批准日期1987/12/18申请机构NOVARTIS PHARMACEUTICALS CORP
化学类型New dosage form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
018927048APLabel2012/12/13下载
018927048APLetter2012/12/13下载
018927047APLetter2011/11/10下载
018927046APLetter2013/03/08下载
018927046APLabel2013/03/08下载
018927044APLetter2014/01/17下载
018927044APLabel2014/01/17下载
018927043APLetter2009/05/01下载
018927043APLabel2009/05/12下载
018927042APMedication Guide2011/03/07下载
018927042APLetter2011/03/07下载
018927042APLabel2011/03/07下载
018927041APMedication Guide2011/03/07下载
018927041APLabel2011/03/07下载
018927041APLetter2011/03/07下载
018927040APLetter2014/09/17下载
018927040APLabel2014/09/19下载
018927039APLabel2007/12/12下载
018927039APLetter2008/01/09下载
018927038APLetter2015/09/01下载
018927038APLabel2015/09/03下载
018927035APLabel2007/08/17下载
018927035APLetter2007/08/17下载
018927031APLetter2001/03/07下载
018927031APLabel2001/03/07下载
018927000APMedication Guide2012/12/18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
018927054AP2016/09/28Manufacturing Change or Addition
018927053AP2016/08/19Manufacturing Change or Addition
018927052AP2016/07/08Manufacturing Change or Addition
018927051AP2016/06/17Manufacturing Change or Addition
018927049AP2013/11/08Manufacturing Change or Addition
018927048AP2012/12/11Labeling Revision
018927047AP2011/10/30Labeling Revision
018927046AP2013/03/06Labeling Revision
018927044AP2014/01/16Labeling Revision
018927043AP2009/04/23Labeling Revision
018927042AP2011/03/03Labeling Revision
018927041AP2011/03/03Labeling Revision
018927040AP2014/09/16Labeling Revision
018927039AP2007/12/11Labeling Revision
018927038AP2015/08/28Labeling Revision
018927035AP2007/08/16Labeling Revision
018927034AP2002/12/11Manufacturing Change or Addition
018927033AP2002/01/28Control Supplement
018927032AP2001/11/15Manufacturing Change or Addition
018927031AP2001/03/07Labeling Revision
018927030AP2000/04/11Manufacturing Change or Addition
018927029AP2000/03/08Manufacturing Change or Addition
018927028AP2000/04/10Labeling Revision
018927027AP1998/12/29Control Supplement
018927026AP1999/02/19Manufacturing Change or Addition
018927025AP1998/07/15Labeling Revision
018927024AP2000/04/10Labeling Revision
018927023AP1998/07/15Labeling Revision
018927022AP1997/01/02Control Supplement
018927021AP1998/07/15Labeling Revision
018927020AP1998/07/15Labeling Revision
018927019AP1995/08/09Manufacturing Change or Addition
018927018AP1995/10/11Patient Population Altered
018927016AP1993/10/06Control Supplement
018927010AP1991/03/14Control Supplement
018927008AP1990/03/26Labeling Revision
018927006AP1989/08/01Manufacturing Change or Addition
018927005AP1989/07/21Labeling Revision
018927004AP1989/04/07Package Change
018927003AP1988/08/01Labeling Revision
018927002AP1988/07/28Manufacturing Change or Addition
018927001AP1988/07/28Manufacturing Change or Addition
018927000AP1987/12/18Approval