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=NDA211617"
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
72426-818-99 72426-818 HUMAN PRESCRIPTION DRUG Nexlizet Bempedoic Acid and Ezetimibe TABLET, FILM COATED ORAL 20200309 N/A NDA NDA211617 Esperion Therapeutics, Inc. BEMPEDOIC ACID; EZETIMIBE 180 mg/1; 10 mg/1 7 TABLET, FILM COATED in 1 BLISTER PACK (72426-818-99)
72426-818-09 72426-818 HUMAN PRESCRIPTION DRUG Nexlizet Bempedoic Acid and Ezetimibe TABLET, FILM COATED ORAL 20200309 N/A NDA NDA211617 Esperion Therapeutics, Inc. BEMPEDOIC ACID; EZETIMIBE 180 mg/1; 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72426-818-09)
72426-818-03 72426-818 HUMAN PRESCRIPTION DRUG Nexlizet Bempedoic Acid and Ezetimibe TABLET, FILM COATED ORAL 20200309 N/A NDA NDA211617 Esperion Therapeutics, Inc. BEMPEDOIC ACID; EZETIMIBE 180 mg/1; 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72426-818-03)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase