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
62332-350-30	62332-350	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Inc.	FENOFIBRATE	54 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-350-30)
62332-350-71	62332-350	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Inc.	FENOFIBRATE	54 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62332-350-71)
62332-350-90	62332-350	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Inc.	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-350-90)
62332-351-30	62332-351	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-351-30)
62332-351-71	62332-351	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62332-351-71)
62332-351-90	62332-351	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-351-90)
46708-350-30	46708-350	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Limited	FENOFIBRATE	54 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-350-30)
46708-350-71	46708-350	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Limited	FENOFIBRATE	54 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (46708-350-71)
46708-350-90	46708-350	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Limited	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-350-90)
46708-351-30	46708-351	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Limited	FENOFIBRATE	160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-351-30)
46708-351-71	46708-351	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Limited	FENOFIBRATE	160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (46708-351-71)
46708-351-90	46708-351	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA213252	Alembic Pharmaceuticals Limited	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-351-90)