药品名称DEXTROSE 5% AND ELECTROLYTE NO. 75 IN PLASTIC CONTAINER
申请号018840产品号001
活性成分DEXTROSE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM LACTATE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格5GM/100ML;205MG/100ML;100MG/100ML;120MG/100ML;220MG/100ML
治疗等效代码参比药物
批准日期1983/06/29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
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
018840029APLabel2005/08/31下载
018840029APLetter2005/08/31下载
018840028APLetter2005/06/08下载
018840028APLabel2005/06/08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
018840029AP2005/08/26Package Change
018840028AP2005/06/07Labeling Revision
018840025AP2001/08/14Manufacturing Change or Addition
018840024AP1999/11/24Manufacturing Change or Addition
018840023AP2000/11/29Labeling Revision
018840022AP1997/04/29Package Change
018840021AP1994/02/18Control Supplement
018840020AP1994/09/30Control Supplement
018840018AP1991/04/26Control Supplement
018840017AP1991/04/29Control Supplement
018840016AP1991/03/26Control Supplement
018840015AP1991/02/15Control Supplement
018840014AP1989/07/26Control Supplement
018840013AP1989/01/12Control Supplement
018840011AP1987/07/25Package Change
018840010AP1987/05/28Control Supplement
018840007AP1986/02/27Package Change
018840006AP1985/04/26Control Supplement
018840004AP1985/04/17Labeling Revision
018840003AP1985/06/13Control Supplement
018840002AP1984/09/22Control Supplement
018840001AP1985/06/24Control Supplement
018840000AP1983/06/29Approval