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
72603-143-03	72603-143	HUMAN PRESCRIPTION DRUG	Metoprolol succinate	Metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230912	N/A	ANDA	ANDA090617	Northstar Rx LLC	METOPROLOL SUCCINATE	50 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-03)
60687-402-01	60687-402	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, EXTENDED RELEASE	ORAL	20181207	N/A	ANDA	ANDA090617	American Health Packaging	METOPROLOL SUCCINATE	50 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-402-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-402-11)
60687-402-65	60687-402	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, EXTENDED RELEASE	ORAL	20230308	N/A	ANDA	ANDA090617	American Health Packaging	METOPROLOL SUCCINATE	50 mg/1	50 BLISTER PACK in 1 CARTON (60687-402-65) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-402-11)
50268-541-15	50268-541	HUMAN PRESCRIPTION DRUG	Metoprolol succinate	Metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180725	N/A	ANDA	ANDA090617	AvPAK	METOPROLOL SUCCINATE	50 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-541-15) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (50268-541-11)