药品名称POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
申请号018876产品号004
活性成分DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格5GM/100ML;298MG/100ML;300MG/100ML
治疗等效代码参比药物
批准日期1988/03/28申请机构HOSPIRA INC
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)
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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
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
018876045AP2013/09/05Manufacturing Change or Addition
018876024AP2001/08/24Labeling Revision
018876023AP1998/10/29Control Supplement
018876021AP1997/06/11Manufacturing Change or Addition
018876020AP1997/08/20Labeling Revision
018876019AP1996/08/06Control Supplement
018876018AP1996/03/04Control Supplement
018876017AP1995/08/18Manufacturing Change or Addition
018876016AP1996/08/29Control Supplement
018876015AP1996/08/27Control Supplement
018876013AP1992/01/28Package Change
018876012AP1991/09/10Control Supplement
018876010AP1990/01/11Manufacturing Change or Addition
018876009AP1990/02/22Manufacturing Change or Addition
018876007AP1987/08/31Expiration Date Change
018876006AP1988/03/28Labeling Revision
018876005AP1988/03/28Control Supplement
018876003AP1989/06/22Control Supplement
018876002AP1986/08/11Control Supplement
018876001AP1986/10/09Control Supplement
018876000AP1986/01/17Approval