TRAVASOL 3.5% W/ ELECTROLYTES(AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE)

药品名称	TRAVASOL 3.5% W/ ELECTROLYTES
申请号	017493	产品号	003
活性成分	AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE	市场状态	停止上市
剂型或给药途径	INJECTABLE;INJECTION	规格	3.5%;51MG/100ML;131MG/100ML;218MG/100ML;35MG/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	BAXTER HEALTHCARE CORP
化学类型	New formulation or new manufacturer	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
017493	067	AP	Letter	2003/01/17	下载
017493	066	AP	Letter	2003/05/30	下载
017493	065	AP	Letter	2003/01/03	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
017493	067	AP	2003/01/17	Control Supplement
017493	066	AP	2003/04/30	Labeling Revision
017493	065	AP	2003/01/03	Labeling Revision
017493	064	AP	1999/03/31	Control Supplement
017493	063	AP	1999/04/05	Control Supplement
017493	062	AP	1994/02/18	Control Supplement
017493	061	AP	1994/05/19	Manufacturing Change or Addition
017493	060	AP	1994/09/30	Control Supplement
017493	059	AP	1992/08/24	Manufacturing Change or Addition
017493	058	AP	1991/04/03	Control Supplement
017493	057	AP	1992/09/14	Control Supplement
017493	056	AP	1993/03/12	Labeling Revision
017493	055	AP	1991/03/26	Control Supplement
017493	054	AP	1990/05/04	Control Supplement
017493	053	AP	1993/03/12	Labeling Revision
017493	052	AP	1997/04/30	Package Change
017493	051	AP	1989/07/26	Control Supplement
017493	049	AP	1987/12/30	Package Change
017493	048	AP	1987/11/18	Labeling Revision
017493	047	AP	1987/07/25	Package Change
017493	046	AP	1985/09/20	Labeling Revision
017493	045	AP	1984/02/28	Control Supplement
017493	043	AP	1983/01/19	Labeling Revision
017493	042	AP	1983/01/19	Control Supplement
017493	041	AP	1985/01/24	Control Supplement
017493	039	AP	1982/07/21	Manufacturing Change or Addition
017493	038	AP	1982/03/08	Control Supplement
017493	037	AP	1982/04/06	Labeling Revision
017493	036	AP	1982/04/06	Control Supplement
017493	035	AP	1982/02/16	Control Supplement
017493	034	AP	1981/12/16	Control Supplement
017493	033	AP	1982/10/15	Labeling Revision
017493	032	AP	1982/10/15	Control Supplement
017493	030	AP	1981/06/29	Control Supplement
017493	029	AP	1981/06/17	Labeling Revision
017493	028	AP	1981/06/17	Formulation Revision
017493	025	AP	1980/07/31	Control Supplement
017493	024	AP	1980/06/03	Control Supplement
017493	023	AP	1979/06/04	Control Supplement
017493	021	AP	1979/04/27	Labeling Revision
017493	020	AP	1979/11/28	Labeling Revision
017493	019	AP	1979/11/28	Control Supplement
017493	018	AP	1978/07/28	Control Supplement
017493	017	AP	1978/07/28	Labeling Revision
017493	016	AP	1978/08/29	Control Supplement
017493	015	AP	1977/12/13	Labeling Revision
017493	014	AP	1977/08/18	Control Supplement
017493	013	AP	1977/07/12	Labeling Revision
017493	012	AP	1977/07/12	Control Supplement
017493	011	AP	1977/07/22	Manufacturing Change or Addition
017493	010	AP	1979/05/10	Control Supplement
017493	009	AP	1977/02/07	Control Supplement
017493	008	AP	1977/04/01	Control Supplement
017493	007	AP	1977/04/01	Labeling Revision
017493	006	AP	1977/12/07	Labeling Revision
017493	005	AP	1976/08/24	Control Supplement
017493	004	AP	1976/06/28	Control Supplement
017493	003	AP	1976/09/08	Labeling Revision
017493	001	AP	1976/07/19	Control Supplement
017493	000	AP	1976/03/24	Approval

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