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
70710-1168-1	70710-1168	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20190312	N/A	ANDA	ANDA210028	Zydus Pharmaceuticals USA Inc.	ATENOLOL; CHLORTHALIDONE	100 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (70710-1168-1)
70710-1167-1	70710-1167	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20190312	N/A	ANDA	ANDA210028	Zydus Pharmaceuticals USA Inc.	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (70710-1167-1)
16714-936-01	16714-936	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20190326	N/A	ANDA	ANDA210028	Northstar Rx LLC.	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (16714-936-01)
70771-1373-1	70771-1373	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20190312	N/A	ANDA	ANDA210028	Zydus Lifesciences Limited	ATENOLOL; CHLORTHALIDONE	100 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (70771-1373-1)
16714-937-01	16714-937	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20190326	N/A	ANDA	ANDA210028	Northstar Rx LLC.	ATENOLOL; CHLORTHALIDONE	100 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (16714-937-01)
70771-1372-1	70771-1372	HUMAN PRESCRIPTION DRUG	Atenolol and Chlorthalidone	Atenolol and Chlorthalidone	TABLET	ORAL	20190312	N/A	ANDA	ANDA210028	Zydus Lifesciences Limited	ATENOLOL; CHLORTHALIDONE	50 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (70771-1372-1)