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
16714-226-02	16714-226	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20240904	N/A	ANDA	ANDA091629	NorthStar Rx LLC	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (16714-226-02)
16714-226-04	16714-226	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20240904	N/A	ANDA	ANDA091629	NorthStar Rx LLC	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16714-226-04)
67046-1618-3	67046-1618	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20251202	N/A	ANDA	ANDA091629	Coupler LLC	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1618-3)
63187-602-90	63187-602	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA091629	Proficient Rx LP	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-602-90)