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
29300-401-05	29300-401	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20201214	N/A	ANDA	ANDA213302	Unichem Pharmaceuticals (USA), Inc.	ATENOLOL; CHLORTHALIDONE	100 mg/1; 25 mg/1	500 TABLET in 1 BOTTLE (29300-401-05)
29300-401-01	29300-401	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20201214	N/A	ANDA	ANDA213302	Unichem Pharmaceuticals (USA), Inc.	ATENOLOL; CHLORTHALIDONE	100 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (29300-401-01)
29300-400-05	29300-400	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20201214	N/A	ANDA	ANDA213302	Unichem Pharmaceuticals (USA), Inc.	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	500 TABLET in 1 BOTTLE (29300-400-05)
29300-400-01	29300-400	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20201214	N/A	ANDA	ANDA213302	Unichem Pharmaceuticals (USA), Inc.	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (29300-400-01)
70518-4111-0	70518-4111	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20240625	N/A	ANDA	ANDA213302	REMEDYREPACK INC.	ATENOLOL; CHLORTHALIDONE	100 mg/1; 25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-4111-0)