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
69097-221-02	69097-221	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211291	Cipla USA Inc.	RANOLAZINE	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69097-221-02)
69097-221-03	69097-221	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211291	Cipla USA Inc.	RANOLAZINE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69097-221-03)
69097-221-12	69097-221	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211291	Cipla USA Inc.	RANOLAZINE	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69097-221-12)
69097-222-02	69097-222	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211291	Cipla USA Inc.	RANOLAZINE	1000 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69097-222-02)
69097-222-03	69097-222	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211291	Cipla USA Inc.	RANOLAZINE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69097-222-03)
69097-222-12	69097-222	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190528	N/A	ANDA	ANDA211291	Cipla USA Inc.	RANOLAZINE	1000 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69097-222-12)