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
63304-018-05	63304-018	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211707	Sun Pharmaceutical Industries, Inc.	RANOLAZINE	1000 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-05)
63304-018-28	63304-018	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211707	Sun Pharmaceutical Industries, Inc.	RANOLAZINE	1000 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-28)
63304-018-60	63304-018	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211707	Sun Pharmaceutical Industries, Inc.	RANOLAZINE	1000 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-60)
63304-017-60	63304-017	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211707	Sun Pharmaceutical Industries, Inc.	RANOLAZINE	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-017-60)
63304-017-28	63304-017	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211707	Sun Pharmaceutical Industries, Inc.	RANOLAZINE	500 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-017-28)
63304-017-05	63304-017	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211707	Sun Pharmaceutical Industries, Inc.	RANOLAZINE	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-017-05)