VEINAMINE 8%(AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; SODIUM ACETATE)

药品名称	VEINAMINE 8%
申请号	017957	产品号	001
活性成分	AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; SODIUM ACETATE	市场状态	停止上市
剂型或给药途径	INJECTABLE;INJECTION	规格	8%;61MG/100ML;211MG/100ML;56MG/100ML;388MG/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

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
017957	039	AP	2005/01/12	Control Supplement
017957	036	AP	1999/12/21	Control Supplement
017957	035	AP	1995/02/09	Manufacturing Change or Addition
017957	034	AP	1993/01/11	Manufacturing Change or Addition
017957	033	AP	1993/04/28	Control Supplement
017957	032	AP	2003/04/17	Labeling Revision
017957	030	AP	1990/04/05	Control Supplement
017957	029	AP	1990/04/05	Control Supplement
017957	028	AP	1989/04/10	Manufacturing Change or Addition
017957	027	AP	1987/09/17	Control Supplement
017957	026	AP	1987/04/30	Labeling Revision
017957	025	AP	1987/03/26	Control Supplement
017957	024	AP	1986/04/04	Control Supplement
017957	023	AP	1986/11/28	Control Supplement
017957	022	AP	1986/11/28	Labeling Revision
017957	021	AP	1985/04/23	Labeling Revision
017957	020	AP	1985/04/23	Control Supplement
017957	019	AP	1984/07/27	Control Supplement
017957	017	AP	1985/11/01	Control Supplement
017957	016	AP	1984/01/19	Control Supplement
017957	014	AP	1983/06/22	Labeling Revision
017957	013	AP	1983/06/07	Labeling Revision
017957	012	AP	1982/08/09	Control Supplement
017957	011	AP	1982/05/05	Control Supplement
017957	010	AP	1982/08/09	Labeling Revision
017957	009	AP	1981/07/08	Control Supplement
017957	008	AP	1981/06/17	Control Supplement
017957	005	AP	1979/05/09	Control Supplement
017957	004	AP	1979/04/09	Control Supplement
017957	003	AP	1979/03/26	Control Supplement
017957	000	AP	1978/01/03	Approval