药品名称ZITHROMAX
申请号050710产品号001
活性成分AZITHROMYCIN市场状态处方药
剂型或给药途径FOR SUSPENSION;ORAL规格EQ 100MG BASE/5ML
治疗等效代码AB参比药物
批准日期1995/10/19申请机构PFIZER CHEMICALS DIV PFIZER INC
化学类型New dosage form审评分类Standard 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
62684892018/07/31YPDF格式
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
050710043APLetter2016/05/25下载
050710043APLabel2016/05/25下载
050710039APLetter2013/02/21下载
050710039APLabel2013/02/21下载
050710038APLetter2012/06/08下载
050710038APLabel2012/06/11下载
050710037APLabel2014/06/10下载
050710037APLetter2014/06/11下载
050710034APLetter2012/11/06下载
050710034APLabel2012/11/06下载
050710033APLetter2011/02/03下载
050710033APLabel2011/02/04下载
050710032APLetter2010/08/17下载
050710032APLabel2010/08/19下载
050710028APLetter2009/03/03下载
050710028APLabel2009/04/03下载
050710023APLabel2007/11/07下载
050710023APLetter2007/11/08下载
050710021APLabel2004/01/22下载
050710021APLetter2004/01/22下载
050710020APLetter2003/12/22下载
050710019APLetter2004/04/29下载
050710017APLetter2004/01/22下载
050710017APLabel2004/01/22下载
050710016APLetter2003/07/06下载
050710014APLetter2002/07/22下载
050710011APLetter2002/05/24下载
050710011APLabel2002/05/24下载
050710011APReview2004/06/04下载
050710009APLetter2001/12/14下载
050710009APLabel2001/12/14下载
050710008APLetter2001/12/14下载
050710008APLabel2001/12/14下载
050710007APLetter2002/10/16下载
050710000APOther Important Information from FDA2013/03/12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
050710043AP2016/05/23Labeling Revision
050710039AP2013/02/19Labeling Revision
050710038AP2012/06/06Labeling Revision
050710037AP2014/06/07Labeling Revision
050710034AP2012/11/02Labeling Revision
050710033AP2011/01/28Labeling Revision
050710032AP2010/08/11Labeling Revision
050710028AP2009/02/27Labeling Revision
050710023AP2007/10/25Labeling Revision
050710021AP2004/01/15Labeling Revision
050710020AP2003/12/18Labeling Revision
050710019AP2004/04/27Labeling Revision
050710017AP2004/01/15Labeling Revision
050710016AP2003/06/20Labeling Revision
050710014AP2002/07/22Labeling Revision
050710012AP2001/12/10Manufacturing Change or Addition
050710011AP2002/05/24Labeling Revision
050710009AP2001/12/14New Dosage Regimen
050710008AP2001/12/14New Dosage Regimen
050710007AP2002/10/16Labeling Revision
050710006AP2000/11/11Labeling Revision
050710005AP1999/11/22Manufacturing Change or Addition
050710004AP1999/11/08Package Change
050710003AP1996/03/18Control Supplement
050710002AP1996/03/14Control Supplement
050710001AP1996/12/20Patient Population Altered
050710000AP1995/10/19Approval