药品名称DYRENIUM
申请号013174产品号002
活性成分TRIAMTERENE市场状态处方药
剂型或给药途径CAPSULE;ORAL规格100MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构CONCORDIA PHARMACEUTICALS INC
化学类型New molecular entity (NME)审评分类Priority review drug
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历史专利信息
与本品相关的市场独占权保护信息
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历史市场独占权保护信息
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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
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
013174059AP2002/02/28Manufacturing Change or Addition
013174058AP1994/09/13Labeling Revision
013174057AP1992/12/09Formulation Revision
013174056AP1992/06/03Formulation Revision
013174054AP1990/03/07Labeling Revision
013174053AP1988/11/09Labeling Revision
013174052AP1988/02/02Control Supplement
013174051AP1987/09/29Labeling Revision
013174050AP1987/09/23Control Supplement
013174046AP1982/08/25Labeling Revision
013174045AP1985/10/04Practioner Draft Labeling
013174044AP1980/07/14Labeling Revision
013174043AP1979/11/26Labeling Revision
013174041AP1979/11/12Labeling Revision
013174040AP1981/02/05Formulation Revision
013174039AP1979/08/07Labeling Revision
013174037AP1978/11/16Labeling Revision
013174036AP1978/08/15Labeling Revision
013174035AP1977/12/12Control Supplement
013174034AP1978/01/19Control Supplement
013174033AP1978/01/19Package Change
013174032AP1978/01/19Manufacturing Change or Addition
013174031AP1978/02/17Labeling Revision
013174030AP1978/05/22Labeling Revision
013174029AP1978/05/22Labeling Revision
013174028AP1977/02/14Package Change
013174027AP1977/02/14Package Change
013174024AP1976/11/05Labeling Revision
013174023AP1976/09/03Labeling Revision
013174022AP1976/09/03Labeling Revision
013174021AP1976/01/14Formulation Revision
013174020AP1976/09/03Labeling Revision
013174019AP1976/01/14Labeling Revision
013174018AP1975/06/02Control Supplement
013174017AP1975/06/02Labeling Revision
013174016AP1976/01/14Other Amendment
013174014AP1975/07/24Other Amendment
013174011AP1975/06/02Other Amendment
013174000AP1964/08/10Approval