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=ANDA076520"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
72162-2152-9 72162-2152 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate TABLET, FILM COATED ORAL 20231207 N/A ANDA ANDA076520 Bryant Ranch Prepack FENOFIBRATE 160 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2152-9)
43353-898-19 43353-898 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate TABLET, FILM COATED ORAL 20140306 N/A ANDA ANDA076520 Aphena Pharma Solutions - Tennessee, LLC FENOFIBRATE 160 mg/1 3060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-898-19)
0378-7100-77 0378-7100 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate TABLET, FILM COATED ORAL 20091222 N/A ANDA ANDA076520 Mylan Pharmaceuticals Inc. FENOFIBRATE 54 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7100-77)
0378-7101-77 0378-7101 HUMAN PRESCRIPTION DRUG Fenofibrate fenofibrate TABLET, FILM COATED ORAL 20091222 N/A ANDA ANDA076520 Mylan Pharmaceuticals Inc. FENOFIBRATE 160 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7101-77)
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