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
68462-714-05	68462-714	HUMAN PRESCRIPTION DRUG	rufinamide	rufinamide	TABLET, FILM COATED	ORAL	20160516	N/A	ANDA	ANDA205075	Glenmark Pharmaceuticals Inc., USA	RUFINAMIDE	400 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-714-05)
68462-714-08	68462-714	HUMAN PRESCRIPTION DRUG	rufinamide	rufinamide	TABLET, FILM COATED	ORAL	20160516	N/A	ANDA	ANDA205075	Glenmark Pharmaceuticals Inc., USA	RUFINAMIDE	400 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68462-714-08)
68462-713-30	68462-713	HUMAN PRESCRIPTION DRUG	rufinamide	rufinamide	TABLET, FILM COATED	ORAL	20160516	N/A	ANDA	ANDA205075	Glenmark Pharmaceuticals Inc., USA	RUFINAMIDE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-713-30)
68462-713-08	68462-713	HUMAN PRESCRIPTION DRUG	rufinamide	rufinamide	TABLET, FILM COATED	ORAL	20160516	N/A	ANDA	ANDA205075	Glenmark Pharmaceuticals Inc., USA	RUFINAMIDE	200 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68462-713-08)
68462-713-05	68462-713	HUMAN PRESCRIPTION DRUG	rufinamide	rufinamide	TABLET, FILM COATED	ORAL	20160516	N/A	ANDA	ANDA205075	Glenmark Pharmaceuticals Inc., USA	RUFINAMIDE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-713-05)