药品名称NORPACE
申请号017447产品号002
活性成分DISOPYRAMIDE PHOSPHATE市场状态处方药
剂型或给药途径CAPSULE;ORAL规格EQ 150MG BASE
治疗等效代码AB参比药物
批准日期Approved Prior to Jan 1, 1982申请机构GD SEARLE LLC
化学类型New molecular entity (NME)审评分类Priority review drug
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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
017447055AP2000/05/17Labeling Revision
017447054AP1998/11/10Labeling Revision
017447053AP1998/07/17Control Supplement
017447052AP1998/02/03Labeling Revision
017447051AP1997/01/13Manufacturing Change or Addition
017447050AP1996/06/28Labeling Revision
017447049AP1996/02/09Package Change
017447048AP1991/07/03New or Modified Indication
017447047AP1992/01/16Labeling Revision
017447046AP1989/11/16Labeling Revision
017447045AP1989/10/20Labeling Revision
017447044AP1988/02/04Manufacturing Change or Addition
017447043AP1987/08/28Labeling Revision
017447042AP1987/08/28Labeling Revision
017447041AP1987/02/12Labeling Revision
017447039AP1986/05/30Labeling Revision
017447038AP1986/06/04Manufacturing Change or Addition
017447037AP1985/06/18Labeling Revision
017447035AP1985/01/25Manufacturing Change or Addition
017447034AP1985/06/19Labeling Revision
017447033AP1984/02/29Labeling Revision
017447032AP1983/09/14Control Supplement
017447031AP1983/10/03Labeling Revision
017447030AP1983/09/06Control Supplement
017447028AP1983/06/10Manufacturing Change or Addition
017447026AP1982/09/21Labeling Revision
017447025AP1985/06/19Labeling Revision
017447024AP1982/06/17Labeling Revision
017447023AP1981/11/30Labeling Revision
017447022AP1981/02/20Labeling Revision
017447021AP1985/06/19Practioner Draft Labeling
017447020AP1981/11/30Labeling Revision
017447019AP1981/01/30Labeling Revision
017447018AP1980/10/17Package Change
017447016AP1980/10/15Control Supplement
017447015AP1980/02/05Package Change
017447014AP1979/11/23Package Change
017447013AP1980/01/30Labeling Revision
017447012AP1980/01/30Labeling Revision
017447011AP1980/01/30Labeling Revision
017447010AP1980/01/30Labeling Revision
017447009AP1980/01/30Labeling Revision
017447008AP1979/04/26Control Supplement
017447006AP1978/09/20Control Supplement
017447003AP1979/07/19General Efficacy (MarkIV)
017447002AP1978/03/02Labeling Revision
017447001AP1978/03/02Labeling Revision
017447000AP1977/09/01Approval