药品名称FLUDARA
申请号020038产品号001
活性成分FLUDARABINE PHOSPHATE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格50MG/VIAL
治疗等效代码参比药物
批准日期1991/04/18申请机构GENZYME CORP
化学类型New molecular entity (NME)审评分类Priority review drug
罕用药/孤儿药
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
020038033APLabel2010/07/31下载
020038033APLetter2010/08/02下载
020038032APLabel2009/02/12下载
020038032APLetter2009/02/13下载
020038031APLabel2007/12/27下载
020038031APLetter2008/01/09下载
020038028APLabel2003/08/14下载
020038028APLetter2003/08/14下载
020038019APLabel2003/04/21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
020038033AP2010/07/29Labeling Revision
020038032AP2009/02/10Labeling Revision
020038031AP2007/12/20Labeling Revision
020038028AP2003/08/01Efficacy Supplement with Clinical Data to Support
020038025AP2002/05/01Control Supplement
020038024AP2002/05/01Manufacturing Change or Addition
020038023AP2002/03/28Control Supplement
020038022AP2002/07/02Control Supplement
020038021AP2002/07/02Manufacturing Change or Addition
020038020AP2000/03/08Package Change
020038019AP2001/12/03Labeling Revision
020038018AP1996/09/05Control Supplement
020038017AP1999/05/24Labeling Revision
020038015AP1996/01/29Control Supplement
020038014AP1994/09/26Labeling Revision
020038013AP1993/05/21Manufacturing Change or Addition
020038011AP1992/10/28Labeling Revision
020038008AP1993/01/07Manufacturing Change or Addition
020038007AP1993/01/07Control Supplement
020038006AP1992/04/02Labeling Revision
020038005AP1991/12/04Control Supplement
020038003AP1991/12/04Control Supplement
020038000AP1991/04/18Approval