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
67877-668-10	67877-668	HUMAN PRESCRIPTION DRUG	Febuxostat	Febuxostat	TABLET, FILM COATED	ORAL	20211208	N/A	ANDA	ANDA212924	Ascend Laboratories, LLC	FEBUXOSTAT	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (67877-668-10)
67877-668-30	67877-668	HUMAN PRESCRIPTION DRUG	Febuxostat	Febuxostat	TABLET, FILM COATED	ORAL	20211208	N/A	ANDA	ANDA212924	Ascend Laboratories, LLC	FEBUXOSTAT	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67877-668-30)
67877-668-38	67877-668	HUMAN PRESCRIPTION DRUG	Febuxostat	Febuxostat	TABLET, FILM COATED	ORAL	20211208	N/A	ANDA	ANDA212924	Ascend Laboratories, LLC	FEBUXOSTAT	40 mg/1	10 BLISTER PACK in 1 CARTON (67877-668-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK
67877-668-90	67877-668	HUMAN PRESCRIPTION DRUG	Febuxostat	Febuxostat	TABLET, FILM COATED	ORAL	20211208	N/A	ANDA	ANDA212924	Ascend Laboratories, LLC	FEBUXOSTAT	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (67877-668-90)
67877-669-01	67877-669	HUMAN PRESCRIPTION DRUG	Febuxostat	Febuxostat	TABLET, FILM COATED	ORAL	20211208	N/A	ANDA	ANDA212924	Ascend Laboratories, LLC	FEBUXOSTAT	80 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (67877-669-01)
67877-669-10	67877-669	HUMAN PRESCRIPTION DRUG	Febuxostat	Febuxostat	TABLET, FILM COATED	ORAL	20211208	N/A	ANDA	ANDA212924	Ascend Laboratories, LLC	FEBUXOSTAT	80 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (67877-669-10)
67877-669-30	67877-669	HUMAN PRESCRIPTION DRUG	Febuxostat	Febuxostat	TABLET, FILM COATED	ORAL	20211208	N/A	ANDA	ANDA212924	Ascend Laboratories, LLC	FEBUXOSTAT	80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67877-669-30)
67877-669-38	67877-669	HUMAN PRESCRIPTION DRUG	Febuxostat	Febuxostat	TABLET, FILM COATED	ORAL	20211208	N/A	ANDA	ANDA212924	Ascend Laboratories, LLC	FEBUXOSTAT	80 mg/1	10 BLISTER PACK in 1 CARTON (67877-669-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK