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
64842-1025-1	64842-1025	HUMAN PRESCRIPTION DRUG	LONSURF	trifluridine and tipiracil	TABLET, FILM COATED	ORAL	20151007	N/A	NDA	NDA207981	Taiho Pharmaceutical Co., Ltd.	TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE	6.14 mg/1; 15 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (64842-1025-1)
64842-1025-2	64842-1025	HUMAN PRESCRIPTION DRUG	LONSURF	trifluridine and tipiracil	TABLET, FILM COATED	ORAL	20151111	N/A	NDA	NDA207981	Taiho Pharmaceutical Co., Ltd.	TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE	6.14 mg/1; 15 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (64842-1025-2)
64842-1025-3	64842-1025	HUMAN PRESCRIPTION DRUG	LONSURF	trifluridine and tipiracil	TABLET, FILM COATED	ORAL	20151021	N/A	NDA	NDA207981	Taiho Pharmaceutical Co., Ltd.	TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE	6.14 mg/1; 15 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (64842-1025-3)
64842-1020-3	64842-1020	HUMAN PRESCRIPTION DRUG	LONSURF	trifluridine and tipiracil	TABLET, FILM COATED	ORAL	20151021	N/A	NDA	NDA207981	Taiho Pharmaceutical Co., Ltd.	TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE	8.19 mg/1; 20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (64842-1020-3)
64842-1020-2	64842-1020	HUMAN PRESCRIPTION DRUG	LONSURF	trifluridine and tipiracil	TABLET, FILM COATED	ORAL	20151111	N/A	NDA	NDA207981	Taiho Pharmaceutical Co., Ltd.	TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE	8.19 mg/1; 20 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (64842-1020-2)
64842-1020-1	64842-1020	HUMAN PRESCRIPTION DRUG	LONSURF	trifluridine and tipiracil	TABLET, FILM COATED	ORAL	20151007	N/A	NDA	NDA207981	Taiho Pharmaceutical Co., Ltd.	TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE	8.19 mg/1; 20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (64842-1020-1)