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
72626-2701-1	72626-2701	HUMAN PRESCRIPTION DRUG	Sofosbuvir and Velpatasvir	Velpatasvir and Sofosbuvir	TABLET, FILM COATED	ORAL	20181114	N/A	NDA AUTHORIZED GENERIC	NDA208341	Asegua Therapeutics LLC	SOFOSBUVIR; VELPATASVIR	400 mg/1; 100 mg/1	2 BLISTER PACK in 1 CARTON (72626-2701-1) / 14 TABLET, FILM COATED in 1 BLISTER PACK
61958-2201-1	61958-2201	HUMAN PRESCRIPTION DRUG	Epclusa	Velpatasvir and Sofosbuvir	TABLET, FILM COATED	ORAL	20160628	N/A	NDA	NDA208341	Gilead Sciences, Inc.	SOFOSBUVIR; VELPATASVIR	400 mg/1; 100 mg/1	28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61958-2201-1)
61958-2203-1	61958-2203	HUMAN PRESCRIPTION DRUG	Epclusa	Velpatasvir and Sofosbuvir	TABLET, FILM COATED	ORAL	20200319	N/A	NDA	NDA208341	Gilead Sciences, Inc.	SOFOSBUVIR; VELPATASVIR	200 mg/1; 50 mg/1	28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61958-2203-1)