药品名称AUGMENTIN '200'
申请号050726产品号001
活性成分AMOXICILLIN; CLAVULANATE POTASSIUM市场状态处方药
剂型或给药途径TABLET, CHEWABLE;ORAL规格200MG;EQ 28.5MG BASE
治疗等效代码AB参比药物
批准日期1996/05/31申请机构DR REDDYS LABORATORIES 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
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
050726024APLabel2013/01/23下载
050726024APLetter2013/01/24下载
050726022APLabel2013/01/23下载
050726022APLetter2013/01/24下载
050726021APLetter2011/10/04下载
050726021APLabel2011/10/18下载
050726020APLabel2008/03/27下载
050726020APLetter2008/04/02下载
050726019APLabel2008/12/08下载
050726019APLetter2008/12/11下载
050726018APLetter2004/08/12下载
050726017APLetter2004/06/07下载
050726014APLetter2003/06/08下载
050726004APLetter2004/05/27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
050726024AP2013/01/22Labeling Revision
050726022AP2013/01/22Labeling Revision
050726021AP2011/09/29Labeling Revision
050726020AP2008/03/27Labeling Revision
050726019AP2008/12/04Labeling Revision
050726018AP2004/08/11Labeling Revision
050726017AP2004/06/03Labeling Revision
050726016AP2002/10/17Control Supplement
050726015AP2002/12/04Control Supplement
050726014AP2003/05/12Labeling Revision
050726012AP2002/03/28Control Supplement
050726011AP2001/04/17Control Supplement
050726010AP2001/03/29Control Supplement
050726009AP2001/05/03Manufacturing Change or Addition
050726007AP1999/11/19Control Supplement
050726006AP1999/09/23Control Supplement
050726005AP1999/02/01Control Supplement
050726004AP2002/04/10Labeling Revision
050726003AP1998/02/19Manufacturing Change or Addition
050726002AP1998/02/11Labeling Revision
050726001AP1997/03/19Labeling Revision
050726000AP1996/05/31Approval