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=ANDA207378"
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
69097-894-02 69097-894 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate CAPSULE ORAL 20170330 N/A ANDA ANDA207378 Cipla USA Inc., FENOFIBRATE 67 mg/1 30 CAPSULE in 1 BOTTLE, PLASTIC (69097-894-02)
69097-894-07 69097-894 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate CAPSULE ORAL 20170330 N/A ANDA ANDA207378 Cipla USA Inc., FENOFIBRATE 67 mg/1 100 CAPSULE in 1 BOTTLE, PLASTIC (69097-894-07)
69097-894-15 69097-894 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate CAPSULE ORAL 20170330 N/A ANDA ANDA207378 Cipla USA Inc., FENOFIBRATE 67 mg/1 1000 CAPSULE in 1 BOTTLE, PLASTIC (69097-894-15)
69097-895-02 69097-895 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate CAPSULE ORAL 20170330 N/A ANDA ANDA207378 Cipla USA Inc., FENOFIBRATE 134 mg/1 30 CAPSULE in 1 BOTTLE, PLASTIC (69097-895-02)
69097-895-07 69097-895 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate CAPSULE ORAL 20170330 N/A ANDA ANDA207378 Cipla USA Inc., FENOFIBRATE 134 mg/1 100 CAPSULE in 1 BOTTLE, PLASTIC (69097-895-07)
69097-895-12 69097-895 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate CAPSULE ORAL 20170330 N/A ANDA ANDA207378 Cipla USA Inc., FENOFIBRATE 134 mg/1 500 CAPSULE in 1 BOTTLE, PLASTIC (69097-895-12)
69097-896-02 69097-896 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate CAPSULE ORAL 20170330 N/A ANDA ANDA207378 Cipla USA Inc., FENOFIBRATE 200 mg/1 30 CAPSULE in 1 BOTTLE, PLASTIC (69097-896-02)
69097-896-07 69097-896 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate CAPSULE ORAL 20170330 N/A ANDA ANDA207378 Cipla USA Inc., FENOFIBRATE 200 mg/1 100 CAPSULE in 1 BOTTLE, PLASTIC (69097-896-07)
69097-896-12 69097-896 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate CAPSULE ORAL 20170330 N/A ANDA ANDA207378 Cipla USA Inc., FENOFIBRATE 200 mg/1 500 CAPSULE in 1 BOTTLE, PLASTIC (69097-896-12)
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