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
71335-2531-3	71335-2531	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20241126	N/A	ANDA	ANDA078512	Bryant Ranch Prepack	ATENOLOL	100 mg/1	60 TABLET in 1 BOTTLE (71335-2531-3)
71335-2531-4	71335-2531	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20241126	N/A	ANDA	ANDA078512	Bryant Ranch Prepack	ATENOLOL	100 mg/1	90 TABLET in 1 BOTTLE (71335-2531-4)
71335-2531-5	71335-2531	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20241126	N/A	ANDA	ANDA078512	Bryant Ranch Prepack	ATENOLOL	100 mg/1	20 TABLET in 1 BOTTLE (71335-2531-5)
71335-2531-6	71335-2531	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20241126	N/A	ANDA	ANDA078512	Bryant Ranch Prepack	ATENOLOL	100 mg/1	180 TABLET in 1 BOTTLE (71335-2531-6)
71335-2531-7	71335-2531	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20241126	N/A	ANDA	ANDA078512	Bryant Ranch Prepack	ATENOLOL	100 mg/1	10 TABLET in 1 BOTTLE (71335-2531-7)
51655-104-26	51655-104	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20220909	N/A	ANDA	ANDA078512	Northwind Health Company, LLC	ATENOLOL	100 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-104-26)
51655-104-52	51655-104	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20231019	N/A	ANDA	ANDA078512	Northwind Health Company, LLC	ATENOLOL	100 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-104-52)
70518-3531-2	70518-3531	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20230919	N/A	ANDA	ANDA078512	REMEDYREPACK INC.	ATENOLOL	25 mg/1	30 TABLET in 1 BLISTER PACK (70518-3531-2)
70518-4099-0	70518-4099	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20240612	N/A	ANDA	ANDA078512	REMEDYREPACK INC.	ATENOLOL	100 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-4099-0)