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
71335-0152-8	71335-0152	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA091629	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (71335-0152-8)
72189-012-90	72189-012	HUMAN PRESCRIPTION DRUG	LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE	LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20190717	N/A	ANDA	ANDA091629	Direct_Rx	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-012-90)
72189-288-90	72189-288	HUMAN PRESCRIPTION DRUG	LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE	LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20211026	N/A	ANDA	ANDA091629	DirectRx	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-288-90)
43063-986-30	43063-986	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20120831	N/A	ANDA	ANDA091629	PD-Rx Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-986-30)