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
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
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
017957039APLetter2005/01/13下载
017957032APLetter2003/05/29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
017957039AP2005/01/12Control Supplement
017957036AP1999/12/21Control Supplement
017957035AP1995/02/09Manufacturing Change or Addition
017957034AP1993/01/11Manufacturing Change or Addition
017957033AP1993/04/28Control Supplement
017957032AP2003/04/17Labeling Revision
017957030AP1990/04/05Control Supplement
017957029AP1990/04/05Control Supplement
017957028AP1989/04/10Manufacturing Change or Addition
017957027AP1987/09/17Control Supplement
017957026AP1987/04/30Labeling Revision
017957025AP1987/03/26Control Supplement
017957024AP1986/04/04Control Supplement
017957023AP1986/11/28Control Supplement
017957022AP1986/11/28Labeling Revision
017957021AP1985/04/23Labeling Revision
017957020AP1985/04/23Control Supplement
017957019AP1984/07/27Control Supplement
017957017AP1985/11/01Control Supplement
017957016AP1984/01/19Control Supplement
017957014AP1983/06/22Labeling Revision
017957013AP1983/06/07Labeling Revision
017957012AP1982/08/09Control Supplement
017957011AP1982/05/05Control Supplement
017957010AP1982/08/09Labeling Revision
017957009AP1981/07/08Control Supplement
017957008AP1981/06/17Control Supplement
017957005AP1979/05/09Control Supplement
017957004AP1979/04/09Control Supplement
017957003AP1979/03/26Control Supplement
017957000AP1978/01/03Approval