AMINOSYN 8.5%(AMINO ACIDS) - 美国FDA药品数据库

药品名称	AMINOSYN 8.5%
申请号	017673	产品号	004
活性成分	AMINO ACIDS	市场状态	处方药
剂型或给药途径	INJECTABLE;INJECTION	规格	8.5% (8.5GM/100ML)
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	HOSPIRA INC
化学类型	New dosage form	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
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
017673	069	AP	Letter	2004/03/16	下载
017673	067	AP	Letter	2003/04/15	下载
017673	066	AP	Letter	2004/05/27	下载
017673	065	AP	Letter	2003/06/22	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
017673	091	AP	2016/07/28	Manufacturing Change or Addition
017673	090	AP	2016/01/15	Manufacturing Change or Addition
017673	089	AP	2013/07/31	Manufacturing Change or Addition
017673	069	AP	2004/03/09	Package Change
017673	067	AP	2003/03/28	Control Supplement
017673	066	AP	2002/10/25	Manufacturing Change or Addition
017673	065	AP	2003/06/12	Labeling Revision
017673	064	AP	1997/05/05	Control Supplement
017673	063	AP	1996/08/27	Control Supplement
017673	062	AP	1996/04/04	Manufacturing Change or Addition
017673	061	AP	1994/07/11	Manufacturing Change or Addition
017673	060	AP	1993/12/30	Control Supplement
017673	059	AP	1992/08/18	Manufacturing Change or Addition
017673	058	AP	1992/02/10	Manufacturing Change or Addition
017673	057	AP	1987/07/13	Labeling Revision
017673	056	AP	1987/07/13	Labeling Revision
017673	053	AP	1986/01/31	Control Supplement
017673	052	AP	1985/11/18	Labeling Revision
017673	051	AP	1985/10/26	Control Supplement
017673	050	AP	1985/09/05	Labeling Revision
017673	049	AP	1985/03/11	Labeling Revision
017673	048	AP	1985/03/11	Control Supplement
017673	047	AP	1984/09/05	Labeling Revision
017673	046	AP	1983/10/13	Control Supplement
017673	045	AP	1983/07/05	Control Supplement
017673	044	AP	1983/07/05	Control Supplement
017673	043	AP	1983/11/03	Control Supplement
017673	042	AP	1983/11/03	Control Supplement
017673	041	AP	1982/06/29	Labeling Revision
017673	040	AP	1982/06/29	Manufacturing Change or Addition
017673	039	AP	1982/03/12	Labeling Revision
017673	038	AP	1982/01/20	Labeling Revision
017673	037	AP	1985/04/10	Practioner Draft Labeling
017673	036	AP	1981/05/16	Package Change
017673	035	AP	1981/11/02	Control Supplement
017673	034	AP	1980/10/01	Labeling Revision
017673	033	AP	1981/05/29	Labeling Revision
017673	032	AP	1981/05/29	Control Supplement
017673	031	AP	1980/07/01	Labeling Revision
017673	030	AP	1979/11/26	Control Supplement
017673	029	AP	1979/10/29	Control Supplement
017673	028	AP	1979/09/04	Labeling Revision
017673	027	AP	1979/09/04	Control Supplement
017673	026	AP	1979/05/02	Control Supplement
017673	025	AP	1979/05/16	Labeling Revision
017673	024	AP	1979/05/16	Control Supplement
017673	023	AP	1980/04/01	Control Supplement
017673	022	AP	1978/12/19	Control Supplement
017673	021	AP	1979/01/09	Labeling Revision
017673	020	AP	1978/03/22	Control Supplement
017673	019	AP	1978/03/17	Control Supplement
017673	018	AP	1979/01/09	Control Supplement
017673	016	AP	1977/10/04	Control Supplement
017673	015	AP	1977/07/25	Control Supplement
017673	014	AP	1977/05/13	Control Supplement
017673	012	AP	1977/12/08	Labeling Revision
017673	011	AP	1977/12/08	Formulation Revision
017673	010	AP	1978/01/26	Control Supplement
017673	009	AP	1976/11/02	Labeling Revision
017673	008	AP	1976/09/09	Control Supplement
017673	007	AP	1978/07/26	Control Supplement
017673	006	AP	1978/07/26	Labeling Revision
017673	005	AP	1976/08/27	General Efficacy (MarkIV)
017673	004	AP	1976/08/27	Control Supplement
017673	003	AP	1976/04/05	Control Supplement
017673	002	AP	1978/07/20	Control Supplement
017673	001	AP	1978/07/20	Labeling Revision
017673	000	AP	1975/12/03	Approval

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