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=ANDA210782"
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
13668-439-01 13668-439 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20180701 N/A ANDA ANDA210782 Torrent Pharmaceuticals Limited FENOFIBRATE 134 mg/1 100 CAPSULE in 1 BOTTLE (13668-439-01)
13668-439-05 13668-439 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20180701 N/A ANDA ANDA210782 Torrent Pharmaceuticals Limited FENOFIBRATE 134 mg/1 500 CAPSULE in 1 BOTTLE (13668-439-05)
13668-439-90 13668-439 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20180701 N/A ANDA ANDA210782 Torrent Pharmaceuticals Limited FENOFIBRATE 134 mg/1 90 CAPSULE in 1 BOTTLE (13668-439-90)
13668-440-01 13668-440 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20180701 N/A ANDA ANDA210782 Torrent Pharmaceuticals Limited FENOFIBRATE 67 mg/1 100 CAPSULE in 1 BOTTLE (13668-440-01)
13668-440-05 13668-440 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20180701 N/A ANDA ANDA210782 Torrent Pharmaceuticals Limited FENOFIBRATE 67 mg/1 500 CAPSULE in 1 BOTTLE (13668-440-05)
13668-440-90 13668-440 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20180701 N/A ANDA ANDA210782 Torrent Pharmaceuticals Limited FENOFIBRATE 67 mg/1 90 CAPSULE in 1 BOTTLE (13668-440-90)
13668-438-90 13668-438 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20180701 N/A ANDA ANDA210782 Torrent Pharmaceuticals Limited FENOFIBRATE 200 mg/1 90 CAPSULE in 1 BOTTLE (13668-438-90)
13668-438-05 13668-438 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20180701 N/A ANDA ANDA210782 Torrent Pharmaceuticals Limited FENOFIBRATE 200 mg/1 500 CAPSULE in 1 BOTTLE (13668-438-05)
13668-438-01 13668-438 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate CAPSULE ORAL 20180701 N/A ANDA ANDA210782 Torrent Pharmaceuticals Limited FENOFIBRATE 200 mg/1 100 CAPSULE in 1 BOTTLE (13668-438-01)
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