药品名称PROGRAF
申请号050708产品号002
活性成分TACROLIMUS市场状态处方药
剂型或给药途径CAPSULE;ORAL规格EQ 5MG BASE
治疗等效代码AB参比药物
批准日期1994/04/08申请机构ASTELLAS PHARMA US INC
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
ODE2013/03/29
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
050708045APLetter2015/05/21下载
050708045APLabel2015/05/21下载
050708043APLetter2013/09/09下载
050708043APLabel2013/09/09下载
050708041APLetter2012/08/15下载
050708041APLabel2012/08/15下载
050708040APLetter2012/07/09下载
050708040APLabel2012/07/10下载
050708038APLabel2012/02/06下载
050708038APLetter2012/02/08下载
050708037APLabel2011/07/18下载
050708037APLetter2011/07/19下载
050708036APLetter2011/07/19下载
050708036APLabel2011/07/18下载
050708034APLetter2009/02/18下载
050708034APLabel2009/02/20下载
050708027APLabel2009/05/21下载
050708027APLetter2009/05/27下载
050708027APReview2012/10/11下载
050708027APOther2012/10/11下载
050708026APLabel2006/05/01下载
050708026APLetter2006/05/01下载
050708025APLetter2005/12/16下载
050708024APLetter2006/04/05下载
050708021APLetter2004/06/23下载
050708021APLabel2004/06/23下载
050708016APLabel2003/05/02下载
050708015APLabel2003/05/02下载
050708013APLabel2003/05/02下载
050708010APLabel2004/06/14下载
050708000APReview2003/09/10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
050708045AP2015/05/19Labeling Revision
050708044AP2014/03/19Manufacturing Change or Addition
050708043AP2013/09/04Labeling Revision
050708042AP2013/01/28Manufacturing Change or Addition
050708041AP2012/08/14Labeling Revision
050708040AP2012/07/05Labeling Revision
050708038AP2012/02/06Labeling Revision
050708037AP2011/07/14Labeling Revision
050708036AP2011/07/14Labeling Revision
050708034AP2009/02/13Labeling Revision
050708027AP2009/05/19Labeling Revision
050708026AP2006/04/27Labeling Revision
050708025AP2005/12/13Labeling Revision
050708024AP2006/03/29New or Modified Indication
050708021AP2004/06/16Labeling Revision
050708017AP2002/10/24Control Supplement
050708016AP2001/07/25Labeling Revision
050708015AP2001/07/25Labeling Revision
050708014AP2001/05/08Manufacturing Change or Addition
050708013AP2000/12/01Efficacy Supplement with Clinical Data to Support
050708011AP1998/08/24Formulation Revision
050708010AP1998/08/24Control Supplement
050708009AP1998/04/20Control Supplement
050708008AP1997/04/22New or Modified Indication
050708007AP1997/04/22New Dosage Regimen
050708006AP1996/04/25Labeling Revision
050708005AP1995/06/22Package Change
050708004AP1995/06/22Control Supplement
050708003AP1995/06/22Package Change
050708000AP1994/04/08Approval