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
65162-379-06	65162-379	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210312	N/A	ANDA	ANDA207690	Amneal Pharmaceuticals LLC	RANOLAZINE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-379-06)
65162-376-50	65162-376	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210312	N/A	ANDA	ANDA207690	Amneal Pharmaceuticals LLC	RANOLAZINE	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-376-50)
65162-376-18	65162-376	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210312	N/A	ANDA	ANDA207690	Amneal Pharmaceuticals LLC	RANOLAZINE	500 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-376-18)
65162-376-06	65162-376	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210312	N/A	ANDA	ANDA207690	Amneal Pharmaceuticals LLC	RANOLAZINE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-376-06)
65162-379-18	65162-379	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210312	N/A	ANDA	ANDA207690	Amneal Pharmaceuticals LLC	RANOLAZINE	1000 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-379-18)
65162-379-50	65162-379	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210312	N/A	ANDA	ANDA207690	Amneal Pharmaceuticals LLC	RANOLAZINE	1000 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-379-50)