药品名称RETROVIR
申请号019910产品号001
活性成分ZIDOVUDINE市场状态处方药
剂型或给药途径SYRUP;ORAL规格50MG/5ML
治疗等效代码AA参比药物
批准日期1989/09/28申请机构VIIV HEALTHCARE CO
化学类型New dosage form审评分类
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
019910041APLetter2014/12/31下载
019910041APLabel2015/01/08下载
019910040APLetter2012/06/04下载
019910040APLabel2012/06/06下载
019910039APLabel2011/11/25下载
019910039APLetter2011/12/01下载
019910036APLabel2010/05/18下载
019910036APLetter2010/05/21下载
019910035APLabel2009/11/19下载
019910035APLetter2010/01/07下载
019910033APLetter2008/09/23下载
019910033APLabel2008/09/23下载
019910032APLabel2006/11/16下载
019910032APLetter2006/11/22下载
019910029APLabel2006/05/16下载
019910029APLetter2006/05/18下载
019910027APLetter2003/10/17下载
019910027APLabel2003/10/17下载
019910026APLabel2003/04/04下载
019910026APLetter2002/12/18下载
019910025APLetter2002/02/21下载
019910024APLabel2003/06/10下载
019910021APReview2005/04/19下载
019910021APLetter2001/03/30下载
019910021APLabel2001/03/30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
019910041AP2014/12/23Labeling Revision
019910040AP2012/05/31Labeling Revision
019910039AP2011/11/18Labeling Revision
019910036AP2010/05/17Labeling Revision
019910035AP2009/11/06Patient Population Altered
019910033AP2008/09/19New Dosage Regimen
019910032AP2006/11/15Labeling Revision
019910029AP2006/05/10Labeling Revision
019910027AP2003/10/15Labeling Revision
019910026AP2002/12/18Labeling Revision
019910025AP2002/02/21Labeling Revision
019910024AP2001/10/05Labeling Revision
019910023AP2000/02/01Control Supplement
019910022AP1999/02/26Manufacturing Change or Addition
019910021AP2001/03/30Labeling Revision
019910020AP1998/02/25Manufacturing Change or Addition
019910019AP1998/03/04Labeling Revision
019910018AP1996/10/04New or Modified Indication
019910016AP1995/07/20Labeling Revision
019910015AP1996/10/04New Dosage Regimen
019910013AP1995/02/06Control Supplement
019910012AP1994/10/07Labeling Revision
019910011AP1994/08/08New or Modified Indication
019910010AP1993/08/24Labeling Revision
019910008AP1992/10/19Expiration Date Change
019910007AP1994/08/08Labeling Revision
019910004AP1990/03/02Patient Population Altered
019910003AP1990/01/12New Dosage Regimen
019910002AP1990/05/02Patient Population Altered
019910001AP1990/05/25Labeling Revision
019910000AP1989/09/28Approval