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=NDA022425"
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
0024-4142-00 0024-4142 HUMAN PRESCRIPTION DRUG Multaq Dronedarone TABLET, FILM COATED ORAL 20240601 N/A NDA NDA022425 Sanofi-Aventis U.S. LLC DRONEDARONE 400 mg/1 6 TABLET, FILM COATED in 1 BLISTER PACK (0024-4142-00)
0024-4142-06 0024-4142 HUMAN PRESCRIPTION DRUG Multaq Dronedarone TABLET, FILM COATED ORAL 20090701 N/A NDA NDA022425 Sanofi-Aventis U.S. LLC DRONEDARONE 400 mg/1 8 BLISTER PACK in 1 BOX (0024-4142-06) / 6 TABLET, FILM COATED in 1 BLISTER PACK (0024-4142-00)
0024-4142-60 0024-4142 HUMAN PRESCRIPTION DRUG Multaq Dronedarone TABLET, FILM COATED ORAL 20090701 N/A NDA NDA022425 Sanofi-Aventis U.S. LLC DRONEDARONE 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (0024-4142-60)
55154-8104-2 55154-8104 HUMAN PRESCRIPTION DRUG Multaq Dronedarone TABLET, FILM COATED ORAL 20090701 N/A NDA NDA022425 Cardinal Health 107, LLC DRONEDARONE 400 mg/1 1260 TABLET, FILM COATED in 1 BOTTLE (55154-8104-2)
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