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
42571-324-64	42571-324	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20200601	N/A	ANDA	ANDA211745	Micro Labs Limited	RANOLAZINE	500 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-324-64)
42571-325-11	42571-325	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20200601	N/A	ANDA	ANDA211745	Micro Labs Limited	RANOLAZINE	1000 mg/1	100 BLISTER PACK in 1 CARTON (42571-325-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (42571-325-32)
42571-325-60	42571-325	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20200601	N/A	ANDA	ANDA211745	Micro Labs Limited	RANOLAZINE	1000 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-325-60)
42571-325-64	42571-325	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20200601	N/A	ANDA	ANDA211745	Micro Labs Limited	RANOLAZINE	1000 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-325-64)
42571-324-60	42571-324	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20200601	N/A	ANDA	ANDA211745	Micro Labs Limited	RANOLAZINE	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-324-60)
42571-324-11	42571-324	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20200601	N/A	ANDA	ANDA211745	Micro Labs Limited	RANOLAZINE	500 mg/1	100 BLISTER PACK in 1 CARTON (42571-324-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (42571-324-32)
42571-324-05	42571-324	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, EXTENDED RELEASE	ORAL	20200601	N/A	ANDA	ANDA211745	Micro Labs Limited	RANOLAZINE	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-324-05)