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=ANDA202252"
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
60505-3120-1 60505-3120 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20130726 N/A ANDA ANDA202252 Apotex Corp. FENOFIBRATE 43 mg/1 100 CAPSULE in 1 BOTTLE (60505-3120-1)
60505-3120-3 60505-3120 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20130726 N/A ANDA ANDA202252 Apotex Corp. FENOFIBRATE 43 mg/1 30 CAPSULE in 1 BOTTLE (60505-3120-3)
60505-3121-1 60505-3121 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20130726 N/A ANDA ANDA202252 Apotex Corp. FENOFIBRATE 130 mg/1 100 CAPSULE in 1 BOTTLE (60505-3121-1)
60505-3121-3 60505-3121 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20130726 N/A ANDA ANDA202252 Apotex Corp. FENOFIBRATE 130 mg/1 30 CAPSULE in 1 BOTTLE (60505-3121-3)
60505-3121-5 60505-3121 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20130726 N/A ANDA ANDA202252 Apotex Corp. FENOFIBRATE 130 mg/1 500 CAPSULE in 1 BOTTLE (60505-3121-5)
60505-3121-9 60505-3121 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20130726 N/A ANDA ANDA202252 Apotex Corp. FENOFIBRATE 130 mg/1 90 CAPSULE in 1 BOTTLE (60505-3121-9)
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