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
71205-949-30	71205-949	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20201008	N/A	ANDA	ANDA207803	Proficient Rx LP	FENOFIBRATE	160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-949-30)
71205-949-55	71205-949	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20201008	N/A	ANDA	ANDA207803	Proficient Rx LP	FENOFIBRATE	160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71205-949-55)
71205-949-60	71205-949	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20201008	N/A	ANDA	ANDA207803	Proficient Rx LP	FENOFIBRATE	160 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-949-60)
71205-949-72	71205-949	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20201008	N/A	ANDA	ANDA207803	Proficient Rx LP	FENOFIBRATE	160 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71205-949-72)
71205-949-78	71205-949	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20201008	N/A	ANDA	ANDA207803	Proficient Rx LP	FENOFIBRATE	160 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71205-949-78)
71205-949-90	71205-949	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20201008	N/A	ANDA	ANDA207803	Proficient Rx LP	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-949-90)
35561-343-00	35561-343	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190630	N/A	ANDA	ANDA207803	AustarPharma LLC	FENOFIBRATE	54 mg/1	63784 TABLET, FILM COATED in 1 BOX (35561-343-00)
35561-343-11	35561-343	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190630	N/A	ANDA	ANDA207803	AustarPharma LLC	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (35561-343-11)
35561-343-13	35561-343	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190630	N/A	ANDA	ANDA207803	AustarPharma LLC	FENOFIBRATE	54 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (35561-343-13)
42291-427-50	42291-427	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20230308	N/A	ANDA	ANDA207803	AvKARE	FENOFIBRATE	160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42291-427-50)
42291-427-90	42291-427	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20230308	N/A	ANDA	ANDA207803	AvKARE	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42291-427-90)
69367-254-05	69367-254	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200423	N/A	ANDA	ANDA207803	Westminster Pharmaceuticals, LLC	FENOFIBRATE	160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69367-254-05)
69367-254-09	69367-254	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200423	N/A	ANDA	ANDA207803	Westminster Pharmaceuticals, LLC	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69367-254-09)
35561-344-00	35561-344	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190630	N/A	ANDA	ANDA207803	AustarPharma LLC	FENOFIBRATE	160 mg/1	21631 TABLET, FILM COATED in 1 BOX (35561-344-00)
35561-344-11	35561-344	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190630	N/A	ANDA	ANDA207803	AustarPharma LLC	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (35561-344-11)
35561-344-13	35561-344	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20190630	N/A	ANDA	ANDA207803	AustarPharma LLC	FENOFIBRATE	160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (35561-344-13)