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
65862-163-90	65862-163	HUMAN PRESCRIPTION DRUG	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20070824	N/A	ANDA	ANDA078450	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE	25 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-163-90)
65862-161-90	65862-161	HUMAN PRESCRIPTION DRUG	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20070824	N/A	ANDA	ANDA078450	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE	12.5 mg/1; 10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-161-90)
65862-162-30	65862-162	HUMAN PRESCRIPTION DRUG	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20070824	N/A	ANDA	ANDA078450	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE	12.5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-162-30)
65862-162-90	65862-162	HUMAN PRESCRIPTION DRUG	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20070824	N/A	ANDA	ANDA078450	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE	12.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-162-90)