美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA207293"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
33342-274-07 33342-274 HUMAN PRESCRIPTION DRUG Febuxostat Febuxostat tablets 40 mg FILM ORAL 20190404 N/A ANDA ANDA207293 Macleods Pharmaceuticals Limited FEBUXOSTAT 40 mg/1 30 FILM in 1 BOTTLE (33342-274-07)
33342-274-10 33342-274 HUMAN PRESCRIPTION DRUG Febuxostat Febuxostat tablets 40 mg FILM ORAL 20190404 N/A ANDA ANDA207293 Macleods Pharmaceuticals Limited FEBUXOSTAT 40 mg/1 90 FILM in 1 BOTTLE (33342-274-10)
33342-274-15 33342-274 HUMAN PRESCRIPTION DRUG Febuxostat Febuxostat tablets 40 mg FILM ORAL 20190404 N/A ANDA ANDA207293 Macleods Pharmaceuticals Limited FEBUXOSTAT 40 mg/1 500 FILM in 1 BOTTLE (33342-274-15)
33342-275-07 33342-275 HUMAN PRESCRIPTION DRUG Febuxostat Febuxostat tablets 80 mg FILM ORAL 20190404 N/A ANDA ANDA207293 Macleods Pharmaceuticals Limited FEBUXOSTAT 80 mg/1 30 FILM in 1 BOTTLE (33342-275-07)
33342-275-10 33342-275 HUMAN PRESCRIPTION DRUG Febuxostat Febuxostat tablets 80 mg FILM ORAL 20190404 N/A ANDA ANDA207293 Macleods Pharmaceuticals Limited FEBUXOSTAT 80 mg/1 90 FILM in 1 BOTTLE (33342-275-10)
33342-275-15 33342-275 HUMAN PRESCRIPTION DRUG Febuxostat Febuxostat tablets 80 mg FILM ORAL 20190404 N/A ANDA ANDA207293 Macleods Pharmaceuticals Limited FEBUXOSTAT 80 mg/1 500 FILM in 1 BOTTLE (33342-275-15)
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