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
68462-320-05	68462-320	HUMAN PRESCRIPTION DRUG	Ranolazine	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190705	N/A	ANDA	ANDA211082	Glenmark Pharmaceuticals Inc., USA	RANOLAZINE	1000 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-320-05)
68462-320-60	68462-320	HUMAN PRESCRIPTION DRUG	Ranolazine	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190705	N/A	ANDA	ANDA211082	Glenmark Pharmaceuticals Inc., USA	RANOLAZINE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-320-60)
68462-319-05	68462-319	HUMAN PRESCRIPTION DRUG	Ranolazine	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190705	N/A	ANDA	ANDA211082	Glenmark Pharmaceuticals Inc., USA	RANOLAZINE	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-319-05)
68462-319-60	68462-319	HUMAN PRESCRIPTION DRUG	Ranolazine	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190705	N/A	ANDA	ANDA211082	Glenmark Pharmaceuticals Inc., USA	RANOLAZINE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-319-60)