HYPAQUE(DIATRIZOATE MEGLUMINE) - 美国FDA药品数据库

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	否
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
无
历史专利信息
无

与本品相关的市场独占权保护信息
独占权代码	失效日期
无
历史市场独占权保护信息
无

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
016403	071	AP	Letter	2002/09/30	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
016403	071	AP	2002/09/30	Labeling Revision
016403	070	AP	2001/08/13	Control Supplement
016403	069	AP	1998/08/20	Manufacturing Change or Addition
016403	068	AP	1995/06/15	Labeling Revision
016403	067	AP	1994/03/25	Manufacturing Change or Addition
016403	066	AP	1991/10/03	Labeling Revision
016403	065	AP	1991/10/03	Labeling Revision
016403	064	AP	1991/10/03	Labeling Revision
016403	063	AP	1991/04/24	Control Supplement
016403	062	AP	1989/10/26	Control Supplement
016403	061	AP	1989/06/28	Labeling Revision
016403	060	AP	1989/05/26	Labeling Revision
016403	059	AP	1989/05/19	Labeling Revision
016403	058	AP	1989/04/18	Package Change
016403	057	AP	1989/06/22	Manufacturing Change or Addition
016403	056	AP	1989/06/22	Manufacturing Change or Addition
016403	055	AP	1989/04/11	Manufacturing Change or Addition
016403	054	AP	1988/02/22	Labeling Revision
016403	053	AP	1990/02/26	Manufacturing Change or Addition
016403	052	AP	1986/02/10	Labeling Revision
016403	051	AP	1985/11/22	Labeling Revision
016403	050	AP	1985/04/16	Labeling Revision
016403	049	AP	1985/04/23	Labeling Revision
016403	048	AP	1985/04/19	Labeling Revision
016403	047	AP	1984/11/26	Labeling Revision
016403	046	AP	1988/05/23	Package Change
016403	045	AP	1983/01/25	Expiration Date Change
016403	044	AP	1985/01/14	Package Change
016403	043	AP	1982/10/18	Manufacturing Change or Addition
016403	042	AP	1984/03/12	Practioner Draft Labeling
016403	041	AP	1985/09/11	Package Change
016403	040	AP	1983/02/28	Control Supplement
016403	039	AP	1982/03/18	Package Change
016403	038	AP	1984/03/12	Practioner Draft Labeling
016403	037	AP	1984/01/24	General Efficacy (MarkIV)
016403	036	AP	1982/02/24	Package Change
016403	035	AP	1984/01/16	Practioner Draft Labeling
016403	034	AP	1982/01/18	Control Supplement
016403	033	AP	1983/10/04	Expiration Date Change
016403	032	AP	1981/04/11	Manufacturing Change or Addition
016403	031	AP	1981/04/27	Expiration Date Change
016403	030	AP	1979/04/17	Package Change
016403	029	AP	1979/02/15	Package Change
016403	028	AP	1979/02/15	Control Supplement
016403	027	AP	1979/02/15	Manufacturing Change or Addition
016403	026	AP	1978/01/30	Manufacturing Change or Addition
016403	025	AP	1978/01/30	Manufacturing Change or Addition
016403	024	AP	1978/01/30	Manufacturing Change or Addition
016403	023	AP	1978/07/28	General Efficacy (MarkIV)
016403	022	AP	1977/04/01	Labeling Revision
016403	021	AP	1976/06/02	Manufacturing Change or Addition
016403	020	AP	1976/06/02	Manufacturing Change or Addition
016403	019	AP	1976/06/02	Manufacturing Change or Addition
016403	018	AP	1976/06/25	Labeling Revision
016403	017	AP	1976/06/21	Labeling Revision
016403	012	AP	1975/08/22	Labeling Revision
016403	011	AP	1975/05/29	Control Supplement
016403	010	AP	1975/05/29	Control Supplement
016403	009	AP	1975/05/29	Control Supplement
016403	000	AP	1969/08/21	Approval

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