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
55154-4790-0	55154-4790	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20100513	N/A	ANDA	ANDA077739	Cardinal Health 107, LLC	METOPROLOL TARTRATE	50 mg/1	10 BLISTER PACK in 1 BAG (55154-4790-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
57237-100-01	57237-100	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Rising Pharma Holdings, Inc.	METOPROLOL TARTRATE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (57237-100-01)
57237-100-99	57237-100	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Rising Pharma Holdings, Inc.	METOPROLOL TARTRATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (57237-100-99)
57237-101-01	57237-101	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Rising Pharma Holdings, Inc.	METOPROLOL TARTRATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (57237-101-01)
57237-101-99	57237-101	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Rising Pharma Holdings, Inc.	METOPROLOL TARTRATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (57237-101-99)
57237-102-01	57237-102	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Rising Pharma Holdings, Inc.	METOPROLOL TARTRATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (57237-102-01)
57237-102-99	57237-102	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Rising Pharma Holdings, Inc.	METOPROLOL TARTRATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (57237-102-99)
59651-758-01	59651-758	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20231207	N/A	ANDA	ANDA077739	Aurobindo Pharma Limited	METOPROLOL TARTRATE	37.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-758-01)
59651-760-01	59651-760	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20231207	N/A	ANDA	ANDA077739	Aurobindo Pharma Limited	METOPROLOL TARTRATE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-760-01)
65862-062-01	65862-062	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Aurobindo Pharma Limited	METOPROLOL TARTRATE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-062-01)
65862-062-99	65862-062	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Aurobindo Pharma Limited	METOPROLOL TARTRATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-062-99)
65862-063-01	65862-063	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Aurobindo Pharma Limited	METOPROLOL TARTRATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-063-01)
65862-063-60	65862-063	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Aurobindo Pharma Limited	METOPROLOL TARTRATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-063-60)
65862-063-99	65862-063	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Aurobindo Pharma Limited	METOPROLOL TARTRATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-063-99)
65862-064-01	65862-064	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Aurobindo Pharma Limited	METOPROLOL TARTRATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-064-01)
65862-064-60	65862-064	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Aurobindo Pharma Limited	METOPROLOL TARTRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-064-60)
65862-064-99	65862-064	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20070911	N/A	ANDA	ANDA077739	Aurobindo Pharma Limited	METOPROLOL TARTRATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-064-99)
68071-3941-6	68071-3941	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20260107	N/A	ANDA	ANDA077739	NuCare Pharmaceuticals, Inc.	METOPROLOL TARTRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-3941-6)
68071-4769-1	68071-4769	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20190215	N/A	ANDA	ANDA077739	NuCare Pharmaceuticals,Inc.	METOPROLOL TARTRATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68071-4769-1)
70518-3997-0	70518-3997	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20240126	N/A	ANDA	ANDA077739	REMEDYREPACK INC.	METOPROLOL TARTRATE	100 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3997-0)