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
71335-2945-5	71335-2945	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20251028	N/A	ANDA	ANDA216916	Bryant Ranch Prepack	METOPROLOL SUCCINATE	100 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-5)
71335-2945-6	71335-2945	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20251028	N/A	ANDA	ANDA216916	Bryant Ranch Prepack	METOPROLOL SUCCINATE	100 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-6)
71335-2945-7	71335-2945	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20251028	N/A	ANDA	ANDA216916	Bryant Ranch Prepack	METOPROLOL SUCCINATE	100 mg/1	10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-7)
68788-8869-3	68788-8869	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250430	N/A	ANDA	ANDA216916	Preferred Pharmaceuticals Inc.	METOPROLOL SUCCINATE	50 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8869-3)
68788-8869-6	68788-8869	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250430	N/A	ANDA	ANDA216916	Preferred Pharmaceuticals Inc.	METOPROLOL SUCCINATE	50 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8869-6)
68788-8869-9	68788-8869	HUMAN PRESCRIPTION DRUG	Metoprolol Succinate	Metoprolol Succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250430	N/A	ANDA	ANDA216916	Preferred Pharmaceuticals Inc.	METOPROLOL SUCCINATE	50 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8869-9)