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=NDA021782"
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
64764-805-10 64764-805 HUMAN PRESCRIPTION DRUG Rozerem ramelteon TABLET, FILM COATED ORAL 20050722 N/A NDA NDA021782 Takeda Pharmaceuticals America, Inc. RAMELTEON 8 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (64764-805-10)
64764-805-22 64764-805 HUMAN PRESCRIPTION DRUG Rozerem ramelteon TABLET, FILM COATED ORAL 20050722 N/A NDA NDA021782 Takeda Pharmaceuticals America, Inc. RAMELTEON 8 mg/1 6 CARTON in 1 TRAY (64764-805-22) / 1 BLISTER PACK in 1 CARTON / 2 TABLET, FILM COATED in 1 BLISTER PACK
64764-805-30 64764-805 HUMAN PRESCRIPTION DRUG Rozerem ramelteon TABLET, FILM COATED ORAL 20050722 N/A NDA NDA021782 Takeda Pharmaceuticals America, Inc. RAMELTEON 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (64764-805-30)
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