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
55289-993-30	55289-993	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	19960424	N/A	ANDA	ANDA073665	PD-Rx Pharmaceuticals, Inc.	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (55289-993-30)
55289-993-60	55289-993	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20000508	N/A	ANDA	ANDA073665	PD-Rx Pharmaceuticals, Inc.	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (55289-993-60)
55289-993-90	55289-993	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20090518	N/A	ANDA	ANDA073665	PD-Rx Pharmaceuticals, Inc.	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (55289-993-90)
0591-5783-01	0591-5783	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	19920801	N/A	ANDA	ANDA073665	Actavis Pharma, Inc.	ATENOLOL; CHLORTHALIDONE	100 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (0591-5783-01)
0591-5782-01	0591-5782	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	19920801	N/A	ANDA	ANDA073665	Actavis Pharma, Inc.	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (0591-5782-01)