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
71205-868-78	71205-868	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211217	N/A	ANDA	ANDA211829	Proficient Rx LP	RANOLAZINE	1000 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-78)
71205-868-90	71205-868	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211217	N/A	ANDA	ANDA211829	Proficient Rx LP	RANOLAZINE	1000 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-90)
77771-424-60	77771-424	HUMAN PRESCRIPTION DRUG	RANOLAZINE	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250630	N/A	ANDA	ANDA211829	Radha Pharmaceuticals, Inc	RANOLAZINE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (77771-424-60)
50228-423-05	50228-423	HUMAN PRESCRIPTION DRUG	RANOLAZINE	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190604	N/A	ANDA	ANDA211829	ScieGen Pharmaceuticals, Inc	RANOLAZINE	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (50228-423-05)
50228-423-30	50228-423	HUMAN PRESCRIPTION DRUG	RANOLAZINE	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190604	N/A	ANDA	ANDA211829	ScieGen Pharmaceuticals, Inc	RANOLAZINE	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (50228-423-30)
50228-423-60	50228-423	HUMAN PRESCRIPTION DRUG	RANOLAZINE	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190604	N/A	ANDA	ANDA211829	ScieGen Pharmaceuticals, Inc	RANOLAZINE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (50228-423-60)