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）

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
35561-249-13	35561-249	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA208476	Bostal LLC	FENOFIBRATE	48 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (35561-249-13)
35561-250-10	35561-250	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA208476	Bostal LLC	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (35561-250-10)
35561-250-13	35561-250	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA208476	Bostal LLC	FENOFIBRATE	145 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (35561-250-13)
35561-249-10	35561-249	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA208476	Bostal LLC	FENOFIBRATE	48 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (35561-249-10)
51407-006-90	51407-006	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20241001	N/A	ANDA	ANDA208476	Golden State Medical Supply, Inc.	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (51407-006-90)
51407-005-90	51407-005	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20241001	N/A	ANDA	ANDA208476	Golden State Medical Supply, Inc.	FENOFIBRATE	48 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (51407-005-90)