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
70954-391-10	70954-391	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20211025	N/A	ANDA	ANDA215560	ANI Pharmaceuticals, Inc.	ATENOLOL; CHLORTHALIDONE	100 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (70954-391-10)
70954-390-10	70954-390	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20211025	N/A	ANDA	ANDA215560	ANI Pharmaceuticals, Inc.	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (70954-390-10)
10135-734-01	10135-734	HUMAN PRESCRIPTION DRUG	ATENOLOL AND CHLORTHALIDONE	atenolol and chlorthalidone tablet	TABLET	ORAL	20220301	N/A	ANDA	ANDA215560	MARLEX PHARMACEUTICALS, INC	ATENOLOL; CHLORTHALIDONE	100 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (10135-734-01)
10135-733-01	10135-733	HUMAN PRESCRIPTION DRUG	ATENOLOL AND CHLORTHALIDONE	atenolol and chlorthalidone tablet	TABLET	ORAL	20220301	N/A	ANDA	ANDA215560	MARLEX PHARMACEUTICALS, INC	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (10135-733-01)
70518-3550-0	70518-3550	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20221006	N/A	ANDA	ANDA215560	REMEDYREPACK INC.	ATENOLOL; CHLORTHALIDONE	100 mg/1; 25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-3550-0)