药品名称SODIUM CHLORIDE 3% IN PLASTIC CONTAINER
申请号019022产品号001
活性成分SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格3GM/100ML
治疗等效代码参比药物
批准日期1983/11/01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
019022026APLetter2014/12/30下载
019022026APLabel2015/01/08下载
019022022APLetter2005/08/31下载
019022022APLabel2005/08/31下载
019022021APLetter2005/06/14下载
019022021APLabel2005/06/14下载
019022017APLetter2002/04/03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
019022027AP2014/06/06Manufacturing Change or Addition
019022026AP2014/12/22Labeling Revision
019022022AP2005/08/26Package Change
019022021AP2005/06/09Labeling Revision
019022019AP2001/08/14Manufacturing Change or Addition
019022018AP1999/11/24Manufacturing Change or Addition
019022017AP2002/04/03Labeling Revision
019022016AP1997/04/29Package Change
019022015AP1994/02/18Control Supplement
019022014AP1994/09/30Control Supplement
019022012AP1991/04/29Control Supplement
019022011AP1991/03/26Control Supplement
019022010AP1990/05/24Control Supplement
019022009AP1991/02/15Control Supplement
019022008AP1989/07/26Control Supplement
019022006AP1987/05/28Control Supplement
019022005AP1985/04/26Control Supplement
019022004AP1985/01/26Labeling Revision
019022003AP1985/06/13Control Supplement
019022002AP1984/09/22Control Supplement
019022001AP1984/12/06Control Supplement
019022000AP1983/11/01Approval