药品名称OMEPRAZOLE
申请号022032产品号001
活性成分OMEPRAZOLE市场状态非处方药
剂型或给药途径TABLET, DELAYED RELEASE;ORAL规格20MG
治疗等效代码参比药物
批准日期2007/12/04申请机构DEXCEL PHARMA TECHNOLOGIES LTD
化学类型New formulation or new manufacturer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
90233912025/08/16YPDF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
022032032APLetter2016/02/11下载
022032032APLabel2016/02/11下载
022032029APLetter2015/06/12下载
022032029APLabel2015/06/19下载
022032024APLetter2015/03/10下载
022032024APLabel2015/03/12下载
022032021APLetter2013/08/20下载
022032021APLabel2013/09/19下载
022032020APLabel2014/01/15下载
022032020APLetter2012/10/30下载
022032019APLetter2012/09/11下载
022032016APLetter2012/04/11下载
022032012APLetter2011/07/05下载
022032008APLetter2010/07/23下载
022032003APLetter2009/07/23下载
022032003APLabel2009/07/24下载
022032003APLetter2009/04/07下载
022032000APReview2009/05/28下载
022032000APSummary Review2009/05/28下载
022032000TALetter2007/07/05下载
022032000APLetter2008/01/09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
022032032AP2016/02/10Labeling Revision
022032031AP2016/02/08Manufacturing Change or Addition
022032029AP2015/06/11Labeling Revision
022032028AP2015/06/01Manufacturing Change or Addition
022032027AP2015/03/30Manufacturing Change or Addition
022032026AP2015/08/07Manufacturing Change or Addition
022032025AP2016/01/05Manufacturing Change or Addition
022032024AP2015/03/06Manufacturing Change or Addition
022032023AP2016/08/02Manufacturing Change or Addition
022032022AP2013/09/13Manufacturing Change or Addition
022032021AP2013/08/16Labeling Revision
022032020AP2012/10/29Labeling Revision
022032019AP2012/09/10Labeling Revision
022032016AP2012/04/09Labeling Revision
022032012AP2011/06/27Labeling Revision
022032008AP2010/07/16Labeling Revision
022032003AP2009/04/02Labeling Revision
022032003AP2009/07/16Other
022032000AP2007/12/04Approval
022032000TA2007/06/14Tentative Approval