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
0378-0032-01	0378-0032	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	metoprolol tartrate	TABLET, FILM COATED	ORAL	19931223	N/A	ANDA	ANDA076704	Mylan Pharmaceuticals Inc.	METOPROLOL TARTRATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0032-01)
0378-0032-10	0378-0032	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	metoprolol tartrate	TABLET, FILM COATED	ORAL	19931223	N/A	ANDA	ANDA076704	Mylan Pharmaceuticals Inc.	METOPROLOL TARTRATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0032-10)
0378-0047-01	0378-0047	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	metoprolol tartrate	TABLET, FILM COATED	ORAL	19931223	N/A	ANDA	ANDA076704	Mylan Pharmaceuticals Inc.	METOPROLOL TARTRATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0047-01)
0378-0047-10	0378-0047	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	metoprolol tartrate	TABLET, FILM COATED	ORAL	19931223	N/A	ANDA	ANDA076704	Mylan Pharmaceuticals Inc.	METOPROLOL TARTRATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0047-10)