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
73141-022-02	73141-022	HUMAN PRESCRIPTION DRUG	RANOLAZINE	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250408	N/A	ANDA	ANDA213517	A2A Integrated Pharmaceuticals	RANOLAZINE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (73141-022-02)
72319-022-02	72319-022	HUMAN PRESCRIPTION DRUG	RANOLAZINE	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220615	N/A	ANDA	ANDA213517	i3 Pharmaceuticals, LLC	RANOLAZINE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72319-022-02)
73141-021-02	73141-021	HUMAN PRESCRIPTION DRUG	RANOLAZINE	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250408	N/A	ANDA	ANDA213517	A2A Integrated Pharmaceuticals	RANOLAZINE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (73141-021-02)
72319-021-02	72319-021	HUMAN PRESCRIPTION DRUG	RANOLAZINE	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220615	N/A	ANDA	ANDA213517	i3 Pharmaceuticals, LLC	RANOLAZINE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72319-021-02)
71335-2556-1	71335-2556	HUMAN PRESCRIPTION DRUG	RANOLAZINE	RANOLAZINE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250123	N/A	ANDA	ANDA213517	Bryant Ranch Prepack	RANOLAZINE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2556-1)