药品名称SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
申请号017670产品号001
活性成分SODIUM CHLORIDE市场状态停止上市
剂型或给药途径SOLUTION;IRRIGATION规格450MG/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 WORLDWIDE, 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)
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
017670043APLetter2004/04/20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
017670043AP2004/04/07Labeling Revision
017670042AP1998/02/04Package Change
017670041AP1996/08/27Control Supplement
017670039AP1992/06/30Control Supplement
017670038AP1993/08/24Package Change
017670037AP1988/11/25Control Supplement
017670036AP1985/10/29Control Supplement
017670034AP1986/01/18Control Supplement
017670033AP1984/10/22Control Supplement
017670031AP1984/08/25Control Supplement
017670030AP1986/02/25Control Supplement
017670029AP1984/03/15Package Change
017670028AP1984/03/01Control Supplement
017670027AP1982/06/10Package Change
017670026AP1981/11/06Control Supplement
017670025AP1982/08/31Practioner Draft Labeling
017670024AP1980/10/21Labeling Revision
017670023AP1980/06/06Control Supplement
017670021AP1980/06/06Control Supplement
017670020AP1980/05/23Control Supplement
017670019AP1980/05/28Control Supplement
017670018AP1980/05/05Labeling Revision
017670017AP1981/07/21Control Supplement
017670016AP1980/03/20Control Supplement
017670015AP1980/02/12Control Supplement
017670012AP1979/10/04Control Supplement
017670011AP1979/07/31Package Change
017670010AP1979/07/18Control Supplement
017670009AP1979/01/05Control Supplement
017670008AP1979/04/30Control Supplement
017670007AP1978/06/26Control Supplement
017670006AP1977/04/26Control Supplement
017670005AP1977/07/21Manufacturing Change or Addition
017670004AP1976/04/20Labeling Revision
017670003AP1976/01/30Labeling Revision
017670002AP1975/10/07Control Supplement
017670001AP1976/01/19Control Supplement
017670000AP1975/03/10Approval