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
59651-010-18	59651-010	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221223	N/A	ANDA	ANDA209081	Aurobindo Pharma Limited	RANOLAZINE	1000 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-010-18)
59651-010-60	59651-010	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221223	N/A	ANDA	ANDA209081	Aurobindo Pharma Limited	RANOLAZINE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-010-60)
59651-010-99	59651-010	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221223	N/A	ANDA	ANDA209081	Aurobindo Pharma Limited	RANOLAZINE	1000 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-010-99)
59651-009-99	59651-009	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221223	N/A	ANDA	ANDA209081	Aurobindo Pharma Limited	RANOLAZINE	500 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-009-99)
59651-009-60	59651-009	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221223	N/A	ANDA	ANDA209081	Aurobindo Pharma Limited	RANOLAZINE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-009-60)
59651-009-18	59651-009	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221223	N/A	ANDA	ANDA209081	Aurobindo Pharma Limited	RANOLAZINE	500 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-009-18)