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
62856-583-52	62856-583	HUMAN PRESCRIPTION DRUG	Banzel	rufinamide	TABLET, FILM COATED	ORAL	20081114	N/A	NDA	NDA021911	Eisai Inc.	RUFINAMIDE	400 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (62856-583-52)
62856-583-14	62856-583	HUMAN PRESCRIPTION DRUG	Banzel	rufinamide	TABLET, FILM COATED	ORAL	20180808	N/A	NDA	NDA021911	Eisai Inc.	RUFINAMIDE	400 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (62856-583-14)
62856-582-52	62856-582	HUMAN PRESCRIPTION DRUG	Banzel	rufinamide	TABLET, FILM COATED	ORAL	20081114	N/A	NDA	NDA021911	Eisai Inc.	RUFINAMIDE	200 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (62856-582-52)
62856-582-04	62856-582	HUMAN PRESCRIPTION DRUG	Banzel	rufinamide	TABLET, FILM COATED	ORAL	20180808	N/A	NDA	NDA021911	Eisai Inc.	RUFINAMIDE	200 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (62856-582-04)
75929-098-12	75929-098	HUMAN PRESCRIPTION DRUG	Banzel	rufinamide	TABLET, FILM COATED	ORAL	20081114	N/A	NDA	NDA021911	Pharma Packaging Solutions, LLC dba Tjoapack LLC	RUFINAMIDE	400 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (75929-098-12)
75929-098-51	75929-098	HUMAN PRESCRIPTION DRUG	Banzel	rufinamide	TABLET, FILM COATED	ORAL	20081114	N/A	NDA	NDA021911	Pharma Packaging Solutions, LLC dba Tjoapack LLC	RUFINAMIDE	400 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (75929-098-51)