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
59651-576-90	59651-576	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20220927	N/A	ANDA	ANDA216798	Aurobindo Pharma Limited	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (59651-576-90)
50090-7208-0	50090-7208	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20240805	N/A	ANDA	ANDA216798	A-S Medication Solutions	FENOFIBRATE	160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-7208-0)
50090-7208-1	50090-7208	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20240805	N/A	ANDA	ANDA216798	A-S Medication Solutions	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7208-1)
50090-7209-0	50090-7209	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20240805	N/A	ANDA	ANDA216798	A-S Medication Solutions	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7209-0)
68071-3542-9	68071-3542	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20231129	N/A	ANDA	ANDA216798	NuCare Pharmaceuticals,Inc.	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-3542-9)
50090-7572-0	50090-7572	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20250605	N/A	ANDA	ANDA216798	A-S Medication Solutions	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7572-0)
50090-7572-1	50090-7572	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20250605	N/A	ANDA	ANDA216798	A-S Medication Solutions	FENOFIBRATE	54 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-7572-1)
59651-575-90	59651-575	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20220927	N/A	ANDA	ANDA216798	Aurobindo Pharma Limited	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (59651-575-90)
68788-8861-3	68788-8861	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20250411	N/A	ANDA	ANDA216798	Preferred Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8861-3)
68788-8861-9	68788-8861	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20250411	N/A	ANDA	ANDA216798	Preferred Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8861-9)