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
24979-244-07	24979-244	HUMAN PRESCRIPTION DRUG	TENORMIN	Atenolol	TABLET	ORAL	20240801	N/A	NDA	NDA018240	Upsher-Smith Laboratories, LLC	ATENOLOL	25 mg/1	90 TABLET in 1 BOTTLE (24979-244-07)
52427-430-90	52427-430	HUMAN PRESCRIPTION DRUG	TENORMIN	Atenolol	TABLET	ORAL	20150415	20260930	NDA	NDA018240	Almatica Pharma LLC	ATENOLOL	50 mg/1	90 TABLET in 1 BOTTLE (52427-430-90)
24979-246-07	24979-246	HUMAN PRESCRIPTION DRUG	TENORMIN	Atenolol	TABLET	ORAL	20240801	N/A	NDA	NDA018240	Upsher-Smith Laboratories, LLC	ATENOLOL	100 mg/1	90 TABLET in 1 BOTTLE (24979-246-07)
52427-429-90	52427-429	HUMAN PRESCRIPTION DRUG	TENORMIN	Atenolol	TABLET	ORAL	20150415	20260531	NDA	NDA018240	Almatica Pharma LLC	ATENOLOL	25 mg/1	90 TABLET in 1 BOTTLE (52427-429-90)
24979-245-07	24979-245	HUMAN PRESCRIPTION DRUG	TENORMIN	Atenolol	TABLET	ORAL	20240801	N/A	NDA	NDA018240	Upsher-Smith Laboratories, LLC	ATENOLOL	50 mg/1	90 TABLET in 1 BOTTLE (24979-245-07)
52427-431-90	52427-431	HUMAN PRESCRIPTION DRUG	TENORMIN	Atenolol	TABLET	ORAL	20150415	20260901	NDA	NDA018240	Almatica Pharma LLC	ATENOLOL	100 mg/1	90 TABLET in 1 BOTTLE (52427-431-90)