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
78206-140-02	78206-140	HUMAN PRESCRIPTION DRUG	HYZAAR	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210601	N/A	NDA	NDA020387	Organon LLC	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (78206-140-02)
78206-141-01	78206-141	HUMAN PRESCRIPTION DRUG	HYZAAR	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210601	N/A	NDA	NDA020387	Organon LLC	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (78206-141-01)
78206-141-02	78206-141	HUMAN PRESCRIPTION DRUG	HYZAAR	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210601	N/A	NDA	NDA020387	Organon LLC	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (78206-141-02)
78206-140-01	78206-140	HUMAN PRESCRIPTION DRUG	HYZAAR	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210601	N/A	NDA	NDA020387	Organon LLC	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (78206-140-01)
78206-139-02	78206-139	HUMAN PRESCRIPTION DRUG	HYZAAR	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210601	N/A	NDA	NDA020387	Organon LLC	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (78206-139-02)
78206-139-01	78206-139	HUMAN PRESCRIPTION DRUG	HYZAAR	losartan potassium and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210601	N/A	NDA	NDA020387	Organon LLC	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (78206-139-01)