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=NDA212028"
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
62856-405-10 62856-405 HUMAN PRESCRIPTION DRUG DAYVIGO lemborexant TABLET, FILM COATED ORAL 20200407 N/A NDA NDA212028 Eisai Inc. LEMBOREXANT 5 mg/1 1 BLISTER PACK in 1 CARTON (62856-405-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
62856-405-30 62856-405 HUMAN PRESCRIPTION DRUG DAYVIGO lemborexant TABLET, FILM COATED ORAL 20200407 N/A NDA NDA212028 Eisai Inc. LEMBOREXANT 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62856-405-30)
62856-405-90 62856-405 HUMAN PRESCRIPTION DRUG DAYVIGO lemborexant TABLET, FILM COATED ORAL 20200407 N/A NDA NDA212028 Eisai Inc. LEMBOREXANT 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (62856-405-90)
62856-410-30 62856-410 HUMAN PRESCRIPTION DRUG DAYVIGO lemborexant TABLET, FILM COATED ORAL 20200407 N/A NDA NDA212028 Eisai Inc. LEMBOREXANT 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62856-410-30)
62856-410-90 62856-410 HUMAN PRESCRIPTION DRUG DAYVIGO lemborexant TABLET, FILM COATED ORAL 20200407 N/A NDA NDA212028 Eisai Inc. LEMBOREXANT 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (62856-410-90)
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