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
70518-4228-0	70518-4228	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241105	N/A	ANDA	ANDA216916	REMEDYREPACK INC.	METOPROLOL SUCCINATE	50 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4228-0)
70010-780-10	70010-780	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	25 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-780-10)
70010-781-05	70010-781	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	50 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-781-05)
70010-781-10	70010-781	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	50 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-781-10)
70010-782-01	70010-782	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	100 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-01)
70010-782-05	70010-782	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	100 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-05)
70010-782-10	70010-782	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	100 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-10)
70010-783-01	70010-783	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	200 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-783-01)
70010-783-05	70010-783	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	200 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-783-05)
70010-783-10	70010-783	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	200 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-783-10)
70010-780-05	70010-780	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	25 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-780-05)
70010-780-01	70010-780	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	25 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-780-01)
70010-781-01	70010-781	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231002	N/A	ANDA	ANDA216916	Granules Pharmaceuticals Inc.	METOPROLOL SUCCINATE	50 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-781-01)