药品名称KLOTRIX
申请号017850产品号001
活性成分POTASSIUM CHLORIDE市场状态停止上市
剂型或给药途径TABLET, EXTENDED RELEASE;ORAL规格10MEQ
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构APOTHECON INC DIV BRISTOL MYERS SQUIBB
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
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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
017850028AP1995/10/03Control Supplement
017850027AP1990/10/03Formulation Revision
017850026AP1989/09/19Labeling Revision
017850025AP1988/06/15Control Supplement
017850024AP1988/06/07Package Change
017850023AP1988/08/26Labeling Revision
017850022AP1987/10/01Control Supplement
017850021AP1987/05/15Package Change
017850020AP1987/02/13Package Change
017850019AP1987/03/11Manufacturing Change or Addition
017850018AP1985/10/24Package Change
017850017AP1985/10/24Package Change
017850016AP1985/05/24Package Change
017850015AP1985/07/30Control Supplement
017850014AP1985/05/15Package Change
017850013AP1985/06/14Expiration Date Change
017850012AP1983/06/09Control Supplement
017850011AP1983/06/09Control Supplement
017850010AP1983/05/04Package Change
017850009AP1983/05/04Control Supplement
017850008AP1983/05/04Manufacturing Change or Addition
017850007AP1983/01/04Manufacturing Change or Addition
017850006AP1982/02/04Control Supplement
017850005AP1981/10/01Labeling Revision
017850004AP1984/08/13Practioner Draft Labeling
017850003AP1981/03/17Control Supplement
017850002AP1980/08/14Package Change
017850001AP1980/08/14Package Change
017850000AP1980/05/22Approval