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
71335-2662-3	71335-2662	HUMAN PRESCRIPTION DRUG	losartan potassium and hydrochlorothiazide	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250626	N/A	ANDA	ANDA204832	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2662-3)
71335-2662-4	71335-2662	HUMAN PRESCRIPTION DRUG	losartan potassium and hydrochlorothiazide	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250626	N/A	ANDA	ANDA204832	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2662-4)
71335-2827-1	71335-2827	HUMAN PRESCRIPTION DRUG	losartan potassium and hydrochlorothiazide	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20251023	N/A	ANDA	ANDA204832	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2827-1)
72162-2462-0	72162-2462	HUMAN PRESCRIPTION DRUG	losartan potassium and hydrochlorothiazide	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250221	N/A	ANDA	ANDA204832	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72162-2462-0)
72162-2462-3	72162-2462	HUMAN PRESCRIPTION DRUG	losartan potassium and hydrochlorothiazide	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250221	N/A	ANDA	ANDA204832	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-2462-3)
72162-2462-9	72162-2462	HUMAN PRESCRIPTION DRUG	losartan potassium and hydrochlorothiazide	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250221	N/A	ANDA	ANDA204832	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72162-2462-9)
72162-2461-0	72162-2461	HUMAN PRESCRIPTION DRUG	losartan potassium and hydrochlorothiazide	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250221	N/A	ANDA	ANDA204832	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72162-2461-0)
72162-2461-3	72162-2461	HUMAN PRESCRIPTION DRUG	losartan potassium and hydrochlorothiazide	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250221	N/A	ANDA	ANDA204832	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-2461-3)
72162-2461-9	72162-2461	HUMAN PRESCRIPTION DRUG	losartan potassium and hydrochlorothiazide	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250221	N/A	ANDA	ANDA204832	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72162-2461-9)