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
62135-838-90	62135-838	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20240705	N/A	ANDA	ANDA209660	Chartwell RX, LLC	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62135-838-90)
62332-539-90	62332-539	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190212	N/A	ANDA	ANDA209660	Alembic Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-539-90)
62332-539-91	62332-539	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190212	N/A	ANDA	ANDA209660	Alembic Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-539-91)
62332-554-90	62332-554	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA209660	Alembic Pharmaceuticals Inc.	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-554-90)
46708-554-90	46708-554	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA209660	Alembic Pharmaceuticals Limited	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-554-90)
62332-555-90	62332-555	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA209660	Alembic Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-555-90)
62332-555-91	62332-555	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA209660	Alembic Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-555-91)
46708-555-90	46708-555	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA209660	Alembic Pharmaceuticals Limited	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-555-90)
46708-555-91	46708-555	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA209660	Alembic Pharmaceuticals Limited	FENOFIBRATE	160 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (46708-555-91)
62135-837-90	62135-837	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20240705	N/A	ANDA	ANDA209660	Chartwell RX, LLC	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62135-837-90)
62332-538-90	62332-538	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190212	N/A	ANDA	ANDA209660	Alembic Pharmaceuticals Inc.	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-538-90)