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=NDA021656"
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
63187-940-90 63187-940 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate TABLET ORAL 20171201 N/A NDA AUTHORIZED GENERIC NDA021656 Proficient Rx LP FENOFIBRATE 48 mg/1 90 TABLET in 1 BOTTLE (63187-940-90)
63187-940-60 63187-940 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate TABLET ORAL 20171201 N/A NDA AUTHORIZED GENERIC NDA021656 Proficient Rx LP FENOFIBRATE 48 mg/1 60 TABLET in 1 BOTTLE (63187-940-60)
63187-940-30 63187-940 HUMAN PRESCRIPTION DRUG Fenofibrate Fenofibrate TABLET ORAL 20171201 N/A NDA AUTHORIZED GENERIC NDA021656 Proficient Rx LP FENOFIBRATE 48 mg/1 30 TABLET in 1 BOTTLE (63187-940-30)
0074-3173-90 0074-3173 HUMAN PRESCRIPTION DRUG Tricor Fenofibrate TABLET ORAL 20160205 N/A NDA NDA021656 AbbVie Inc. FENOFIBRATE 48 mg/1 90 TABLET in 1 BOTTLE (0074-3173-90)
0074-3189-90 0074-3189 HUMAN PRESCRIPTION DRUG Tricor Fenofibrate TABLET ORAL 20160205 N/A NDA NDA021656 AbbVie Inc. FENOFIBRATE 145 mg/1 90 TABLET in 1 BOTTLE (0074-3189-90)
50090-2899-2 50090-2899 HUMAN PRESCRIPTION DRUG Tricor Fenofibrate TABLET ORAL 20170303 N/A NDA NDA021656 A-S Medication Solutions FENOFIBRATE 145 mg/1 90 TABLET in 1 BOTTLE (50090-2899-2)
43353-272-30 43353-272 HUMAN PRESCRIPTION DRUG Tricor Fenofibrate TABLET ORAL 20170127 N/A NDA NDA021656 Aphena Pharma Solutions - Tennessee, LLC FENOFIBRATE 145 mg/1 30 TABLET in 1 BOTTLE (43353-272-30)
43353-272-83 43353-272 HUMAN PRESCRIPTION DRUG Tricor Fenofibrate TABLET ORAL 20170127 N/A NDA NDA021656 Aphena Pharma Solutions - Tennessee, LLC FENOFIBRATE 145 mg/1 3600 TABLET in 1 BOTTLE (43353-272-83)
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