药品名称LEUKERAN
申请号010669产品号002
活性成分CHLORAMBUCIL市场状态处方药
剂型或给药途径TABLET;ORAL规格2MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构ASPEN GLOBAL INC
化学类型New molecular entity (NME)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
010669032APLabel2011/11/01下载
010669032APLetter2011/11/03下载
010669030APLetter2010/04/28下载
010669030APLabel2010/05/03下载
010669029APLetter2005/05/25下载
010669028APLetter2003/11/25下载
010669028APLabel2003/12/02下载
010669024APLetter2001/06/20下载
010669023APLetter2001/07/24下载
010669022APLetter2001/07/24下载
010669021APLetter2001/07/24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
010669032AP2011/10/28Labeling Revision
010669030AP2010/04/23Labeling Revision
010669029AP2005/05/24Labeling Revision
010669028AP2003/11/13Labeling Revision
010669025AP2002/11/14Manufacturing Change or Addition
010669024AP2001/06/20Labeling Revision
010669023AP2001/07/24Formulation Revision
010669022AP2001/07/24Control Supplement
010669021AP2001/07/24Manufacturing Change or Addition
010669020AP1995/06/29Control Supplement
010669018AP1994/02/04Manufacturing Change or Addition
010669017AP1996/02/09Labeling Revision
010669016AP1992/10/14Control Supplement
010669015AP1989/02/28Labeling Revision
010669014AP1990/03/06Package Change
010669012AP1986/09/22Labeling Revision
010669011AP1984/03/12Practioner Draft Labeling
010669009AP1981/08/27Labeling Revision
010669008AP1978/06/08Package Change
010669007AP1978/03/22Control Supplement
010669006AP1979/02/15Control Supplement
010669005AP1977/03/09Control Supplement
010669000AP1957/03/18Approval