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
65862-469-30	65862-469	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20101006	N/A	ANDA	ANDA091629	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-469-30)
65862-469-59	65862-469	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20101006	N/A	ANDA	ANDA091629	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	5000 TABLET, FILM COATED in 1 BOTTLE (65862-469-59)
65862-469-90	65862-469	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20101006	N/A	ANDA	ANDA091629	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-469-90)
65862-469-99	65862-469	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20101006	N/A	ANDA	ANDA091629	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-469-99)