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
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)
70518-3293-1	70518-3293	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20211230	N/A	ANDA	ANDA077739	REMEDYREPACK INC.	METOPROLOL TARTRATE	50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3293-1)
70518-3293-2	70518-3293	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20220203	N/A	ANDA	ANDA077739	REMEDYREPACK INC.	METOPROLOL TARTRATE	50 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3293-2)
70518-3293-3	70518-3293	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20220217	N/A	ANDA	ANDA077739	REMEDYREPACK INC.	METOPROLOL TARTRATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3293-3)
43063-821-30	43063-821	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20180627	20270831	ANDA	ANDA077739	PD-Rx Pharmaceuticals, Inc.	METOPROLOL TARTRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-30)
43063-821-60	43063-821	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20180517	20270831	ANDA	ANDA077739	PD-Rx Pharmaceuticals, Inc.	METOPROLOL TARTRATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-60)
43063-821-90	43063-821	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20170105	20270831	ANDA	ANDA077739	PD-Rx Pharmaceuticals, Inc.	METOPROLOL TARTRATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-90)
43063-821-93	43063-821	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20170105	20270831	ANDA	ANDA077739	PD-Rx Pharmaceuticals, Inc.	METOPROLOL TARTRATE	50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-93)
42708-147-60	42708-147	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20210423	N/A	ANDA	ANDA077739	QPharma, Inc.	METOPROLOL TARTRATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-147-60)
71610-080-53	71610-080	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20180531	N/A	ANDA	ANDA077739	Aphena Pharma Solutions - Tennessee, LLC	METOPROLOL TARTRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-080-53)
71610-080-60	71610-080	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20180531	N/A	ANDA	ANDA077739	Aphena Pharma Solutions - Tennessee, LLC	METOPROLOL TARTRATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-080-60)
71610-080-80	71610-080	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20180531	N/A	ANDA	ANDA077739	Aphena Pharma Solutions - Tennessee, LLC	METOPROLOL TARTRATE	100 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71610-080-80)
51655-514-25	51655-514	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20220714	N/A	ANDA	ANDA077739	Northwind Health Company, LLC	METOPROLOL TARTRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-514-25)
51655-514-26	51655-514	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20230407	N/A	ANDA	ANDA077739	Northwind Health Company, LLC	METOPROLOL TARTRATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-514-26)
51655-514-52	51655-514	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20220808	N/A	ANDA	ANDA077739	Northwind Health Company, LLC	METOPROLOL TARTRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-514-52)
51655-514-83	51655-514	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20230106	N/A	ANDA	ANDA077739	Northwind Health Company, LLC	METOPROLOL TARTRATE	100 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-514-83)
71335-0192-1	71335-0192	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate	Metoprolol Tartrate	TABLET, FILM COATED	ORAL	20180309	N/A	ANDA	ANDA077739	Bryant Ranch Prepack	METOPROLOL TARTRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0192-1)
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)