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
62332-360-30	62332-360	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Inc.	FENOFIBRATE	48 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-360-30)
62332-360-71	62332-360	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Inc.	FENOFIBRATE	48 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62332-360-71)
62332-360-90	62332-360	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Inc.	FENOFIBRATE	48 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-360-90)
62332-361-30	62332-361	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Inc.	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-361-30)
62332-361-71	62332-361	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Inc.	FENOFIBRATE	145 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62332-361-71)
62332-361-90	62332-361	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Inc.	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-361-90)
46708-360-30	46708-360	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Limited	FENOFIBRATE	48 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-360-30)
46708-360-71	46708-360	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Limited	FENOFIBRATE	48 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (46708-360-71)
46708-360-90	46708-360	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Limited	FENOFIBRATE	48 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-360-90)
46708-361-30	46708-361	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Limited	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-361-30)
46708-361-71	46708-361	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Limited	FENOFIBRATE	145 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (46708-361-71)
46708-361-90	46708-361	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20190809	N/A	ANDA	ANDA210476	Alembic Pharmaceuticals Limited	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-361-90)