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
65841-023-40	65841-023	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20051008	N/A	ANDA	ANDA076900	Zydus Lifesciences Limited	ATENOLOL	50 mg/1	5000 TABLET in 1 BOTTLE (65841-023-40)
65841-024-01	65841-024	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20051008	N/A	ANDA	ANDA076900	Zydus Lifesciences Limited	ATENOLOL	100 mg/1	100 TABLET in 1 BOTTLE (65841-024-01)
65841-024-10	65841-024	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20051008	N/A	ANDA	ANDA076900	Zydus Lifesciences Limited	ATENOLOL	100 mg/1	1000 TABLET in 1 BOTTLE (65841-024-10)
65841-024-16	65841-024	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20051008	N/A	ANDA	ANDA076900	Zydus Lifesciences Limited	ATENOLOL	100 mg/1	90 TABLET in 1 BOTTLE (65841-024-16)
65841-024-40	65841-024	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20051008	N/A	ANDA	ANDA076900	Zydus Lifesciences Limited	ATENOLOL	100 mg/1	5000 TABLET in 1 BOTTLE (65841-024-40)
43063-952-30	43063-952	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20201018	N/A	ANDA	ANDA076900	PD-Rx Pharmaceuticals, Inc.	ATENOLOL	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (43063-952-30)
43063-952-90	43063-952	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20190228	N/A	ANDA	ANDA076900	PD-Rx Pharmaceuticals, Inc.	ATENOLOL	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (43063-952-90)
60687-605-01	60687-605	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20211025	N/A	ANDA	ANDA076900	American Health Packaging	ATENOLOL	25 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-605-01) / 1 TABLET in 1 BLISTER PACK (60687-605-11)
50090-6779-0	50090-6779	HUMAN PRESCRIPTION DRUG	Atenolol	Atenolol	TABLET	ORAL	20231025	N/A	ANDA	ANDA076900	A-S Medication Solutions	ATENOLOL	50 mg/1	90 TABLET in 1 BOTTLE (50090-6779-0)