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
42658-141-01	42658-141	HUMAN PRESCRIPTION DRUG	IRBESARTAN AND HYDROCHLOROTHIAZIDE	irbesartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA207896	Hisun Pharmaceuticals USA Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42658-141-01)
42658-141-04	42658-141	HUMAN PRESCRIPTION DRUG	IRBESARTAN AND HYDROCHLOROTHIAZIDE	irbesartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA207896	Hisun Pharmaceuticals USA Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42658-141-04)
42658-141-07	42658-141	HUMAN PRESCRIPTION DRUG	IRBESARTAN AND HYDROCHLOROTHIAZIDE	irbesartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA207896	Hisun Pharmaceuticals USA Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42658-141-07)
42658-142-01	42658-142	HUMAN PRESCRIPTION DRUG	IRBESARTAN AND HYDROCHLOROTHIAZIDE	irbesartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA207896	Hisun Pharmaceuticals USA Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42658-142-01)
42658-142-04	42658-142	HUMAN PRESCRIPTION DRUG	IRBESARTAN AND HYDROCHLOROTHIAZIDE	irbesartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA207896	Hisun Pharmaceuticals USA Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42658-142-04)
42658-142-07	42658-142	HUMAN PRESCRIPTION DRUG	IRBESARTAN AND HYDROCHLOROTHIAZIDE	irbesartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA207896	Hisun Pharmaceuticals USA Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42658-142-07)