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=ANDA210721"
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
60505-4632-3 60505-4632 HUMAN PRESCRIPTION DRUG CycloSPORINE, Modfied Cyclosporine CAPSULE, LIQUID FILLED ORAL 20191105 N/A ANDA ANDA210721 Apotex Corp. CYCLOSPORINE 100 mg/1 30 BLISTER PACK in 1 CARTON (60505-4632-3) / 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
60505-4631-3 60505-4631 HUMAN PRESCRIPTION DRUG CycloSPORINE, Modfied Cyclosporine CAPSULE, LIQUID FILLED ORAL 20191105 N/A ANDA ANDA210721 Apotex Corp. CYCLOSPORINE 50 mg/1 30 BLISTER PACK in 1 CARTON (60505-4631-3) / 5 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
60505-4630-3 60505-4630 HUMAN PRESCRIPTION DRUG CycloSPORINE, Modfied Cyclosporine CAPSULE, LIQUID FILLED ORAL 20191105 N/A ANDA ANDA210721 Apotex Corp. CYCLOSPORINE 25 mg/1 30 BLISTER PACK in 1 CARTON (60505-4630-3) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
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