药品名称TAXOL
申请号020262产品号001
活性成分PACLITAXEL市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格6MG/ML
治疗等效代码AP参比药物
批准日期1992/12/29申请机构HQ SPECIALTY PHARMA 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
020262051APLetter2015/03/04下载
020262051APLabel2015/03/05下载
020262049APLabel2011/05/02下载
020262049APLetter2011/05/04下载
020262048APLabel2010/08/28下载
020262048APLetter2010/09/07下载
020262041APLetter2003/03/26下载
020262038APReview2005/12/16下载
020262038APLetter2002/03/04下载
020262037APLetter2002/03/04下载
020262037APReview2005/12/16下载
020262036APReview2005/12/16下载
020262036APLetter2000/06/20下载
020262036APLabel2000/06/20下载
020262035APLetter2002/08/29下载
020262033APLetter1999/10/25下载
020262033APLabel1999/10/25下载
020262031APReview2000/07/06下载
020262028APReview2000/06/15下载
020262028APLetter1998/04/09下载
020262028APLabel1998/04/09下载
020262027APLabel1998/04/09下载
020262027APReview2000/06/15下载
020262027APLetter1998/04/09下载
020262026APLetter1998/04/09下载
020262026APReview2000/06/15下载
020262026APLabel1998/04/09下载
020262024APLetter1998/06/30下载
020262024APReview1999/09/09下载
020262024APLabel1998/06/30下载
020262021APReview1999/01/08下载
020262016APReview1999/01/08下载
020262014APReview1999/01/08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
020262051AP2015/03/03Labeling Revision
020262050AP2014/06/27Manufacturing Change or Addition
020262049AP2011/05/02Labeling Revision
020262048AP2010/08/13Labeling Revision
020262042AP2002/12/12Package Change
020262041AP2003/03/05Labeling Revision
020262040AP2001/05/23Control Supplement
020262039AP2001/04/10Manufacturing Change or Addition
020262038AP2002/03/04Labeling Revision
020262037AP2002/03/04Labeling Revision
020262036AP2000/06/20New Dosage Regimen
020262035AP2002/08/29Labeling Revision
020262033AP1999/10/25New or Modified Indication
020262032AP1999/12/10Labeling Revision
020262031AP1999/01/08Labeling Revision
020262030AP1999/03/19Control Supplement
020262029AP1998/11/05Manufacturing Change or Addition
020262028AP1998/04/09Labeling Revision
020262027AP1998/04/09Labeling Revision
020262026AP1998/04/09New or Modified Indication
020262025AP1997/12/19Control Supplement
020262024AP1998/06/30New or Modified Indication
020262023AP1998/04/01Control Supplement
020262022AP1997/08/04New or Modified Indication
020262021AP1999/01/08Labeling Revision
020262019AP1997/04/25Manufacturing Change or Addition
020262018AP1997/09/18Manufacturing Change or Addition
020262017AP1997/03/05Manufacturing Change or Addition
020262016AP1999/01/08Labeling Revision
020262015AP1996/12/13Package Change
020262014AP1999/01/08Labeling Revision
020262013AP1996/04/03Control Supplement
020262012AP1996/04/01Labeling Revision
020262011AP1995/05/05Formulation Revision
020262010AP1995/02/15Control Supplement
020262009AP1994/07/22Manufacturing Change or Addition
020262008AP1994/10/19Manufacturing Change or Addition
020262007AP1994/04/21Control Supplement
020262005AP1994/03/16Manufacturing Change or Addition
020262004AP1994/04/13New or Modified Indication
020262003AP1994/06/22New Dosage Regimen
020262002AP1993/07/23Labeling Revision
020262001AP1993/06/25Manufacturing Change or Addition
020262000AP1992/12/29Approval