药品名称HYPAQUE
申请号016403产品号002
活性成分DIATRIZOATE MEGLUMINE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格30%
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构GE HEALTHCARE
化学类型New dosage form审评分类Priority 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
016403071APLetter2002/09/30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
016403071AP2002/09/30Labeling Revision
016403070AP2001/08/13Control Supplement
016403069AP1998/08/20Manufacturing Change or Addition
016403068AP1995/06/15Labeling Revision
016403067AP1994/03/25Manufacturing Change or Addition
016403066AP1991/10/03Labeling Revision
016403065AP1991/10/03Labeling Revision
016403064AP1991/10/03Labeling Revision
016403063AP1991/04/24Control Supplement
016403062AP1989/10/26Control Supplement
016403061AP1989/06/28Labeling Revision
016403060AP1989/05/26Labeling Revision
016403059AP1989/05/19Labeling Revision
016403058AP1989/04/18Package Change
016403057AP1989/06/22Manufacturing Change or Addition
016403056AP1989/06/22Manufacturing Change or Addition
016403055AP1989/04/11Manufacturing Change or Addition
016403054AP1988/02/22Labeling Revision
016403053AP1990/02/26Manufacturing Change or Addition
016403052AP1986/02/10Labeling Revision
016403051AP1985/11/22Labeling Revision
016403050AP1985/04/16Labeling Revision
016403049AP1985/04/23Labeling Revision
016403048AP1985/04/19Labeling Revision
016403047AP1984/11/26Labeling Revision
016403046AP1988/05/23Package Change
016403045AP1983/01/25Expiration Date Change
016403044AP1985/01/14Package Change
016403043AP1982/10/18Manufacturing Change or Addition
016403042AP1984/03/12Practioner Draft Labeling
016403041AP1985/09/11Package Change
016403040AP1983/02/28Control Supplement
016403039AP1982/03/18Package Change
016403038AP1984/03/12Practioner Draft Labeling
016403037AP1984/01/24General Efficacy (MarkIV)
016403036AP1982/02/24Package Change
016403035AP1984/01/16Practioner Draft Labeling
016403034AP1982/01/18Control Supplement
016403033AP1983/10/04Expiration Date Change
016403032AP1981/04/11Manufacturing Change or Addition
016403031AP1981/04/27Expiration Date Change
016403030AP1979/04/17Package Change
016403029AP1979/02/15Package Change
016403028AP1979/02/15Control Supplement
016403027AP1979/02/15Manufacturing Change or Addition
016403026AP1978/01/30Manufacturing Change or Addition
016403025AP1978/01/30Manufacturing Change or Addition
016403024AP1978/01/30Manufacturing Change or Addition
016403023AP1978/07/28General Efficacy (MarkIV)
016403022AP1977/04/01Labeling Revision
016403021AP1976/06/02Manufacturing Change or Addition
016403020AP1976/06/02Manufacturing Change or Addition
016403019AP1976/06/02Manufacturing Change or Addition
016403018AP1976/06/25Labeling Revision
016403017AP1976/06/21Labeling Revision
016403012AP1975/08/22Labeling Revision
016403011AP1975/05/29Control Supplement
016403010AP1975/05/29Control Supplement
016403009AP1975/05/29Control Supplement
016403000AP1969/08/21Approval