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
67046-0843-3	67046-0843	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20260427	N/A	ANDA	ANDA078512	Coupler LLC	ATENOLOL	50 mg/1	30 TABLET in 1 BLISTER PACK (67046-0843-3)
50090-5741-0	50090-5741	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20210929	N/A	ANDA	ANDA078512	A-S Medication Solutions	ATENOLOL	50 mg/1	100 TABLET in 1 BOTTLE (50090-5741-0)
50090-5741-1	50090-5741	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20210929	N/A	ANDA	ANDA078512	A-S Medication Solutions	ATENOLOL	50 mg/1	30 TABLET in 1 BOTTLE (50090-5741-1)
50090-5741-4	50090-5741	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20210929	N/A	ANDA	ANDA078512	A-S Medication Solutions	ATENOLOL	50 mg/1	60 TABLET in 1 BOTTLE (50090-5741-4)
50090-5741-7	50090-5741	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20210929	N/A	ANDA	ANDA078512	A-S Medication Solutions	ATENOLOL	50 mg/1	200 TABLET in 1 BOTTLE (50090-5741-7)
50090-5741-8	50090-5741	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20210929	N/A	ANDA	ANDA078512	A-S Medication Solutions	ATENOLOL	50 mg/1	90 TABLET in 1 BOTTLE (50090-5741-8)
67046-1076-3	67046-1076	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20260506	N/A	ANDA	ANDA078512	Coupler LLC	ATENOLOL	100 mg/1	30 TABLET in 1 BLISTER PACK (67046-1076-3)
50090-5738-5	50090-5738	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20210929	N/A	ANDA	ANDA078512	A-S Medication Solutions	ATENOLOL	100 mg/1	90 TABLET in 1 BOTTLE (50090-5738-5)
50090-5738-3	50090-5738	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20210929	N/A	ANDA	ANDA078512	A-S Medication Solutions	ATENOLOL	100 mg/1	60 TABLET in 1 BOTTLE (50090-5738-3)
50090-5738-0	50090-5738	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20210929	N/A	ANDA	ANDA078512	A-S Medication Solutions	ATENOLOL	100 mg/1	30 TABLET in 1 BOTTLE (50090-5738-0)
51655-533-25	51655-533	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20221228	N/A	ANDA	ANDA078512	Northwind Health Company, LLC	ATENOLOL	25 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (51655-533-25)
51655-533-26	51655-533	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20221228	N/A	ANDA	ANDA078512	Northwind Health Company, LLC	ATENOLOL	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-533-26)
51655-533-52	51655-533	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20221228	N/A	ANDA	ANDA078512	Northwind Health Company, LLC	ATENOLOL	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-533-52)
51655-928-52	51655-928	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20220810	N/A	ANDA	ANDA078512	Northwind Health Company, LLC	ATENOLOL	50 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-928-52)
65862-168-01	65862-168	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20071031	N/A	ANDA	ANDA078512	Aurobindo Pharma Limited	ATENOLOL	25 mg/1	100 TABLET in 1 BOTTLE (65862-168-01)
65862-168-99	65862-168	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20071031	N/A	ANDA	ANDA078512	Aurobindo Pharma Limited	ATENOLOL	25 mg/1	1000 TABLET in 1 BOTTLE (65862-168-99)
65862-169-01	65862-169	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20071031	N/A	ANDA	ANDA078512	Aurobindo Pharma Limited	ATENOLOL	50 mg/1	100 TABLET in 1 BOTTLE (65862-169-01)
65862-169-99	65862-169	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20071031	N/A	ANDA	ANDA078512	Aurobindo Pharma Limited	ATENOLOL	50 mg/1	1000 TABLET in 1 BOTTLE (65862-169-99)
65862-170-01	65862-170	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20071031	N/A	ANDA	ANDA078512	Aurobindo Pharma Limited	ATENOLOL	100 mg/1	100 TABLET in 1 BOTTLE (65862-170-01)
65862-170-99	65862-170	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20071031	N/A	ANDA	ANDA078512	Aurobindo Pharma Limited	ATENOLOL	100 mg/1	1000 TABLET in 1 BOTTLE (65862-170-99)