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
65862-617-30	65862-617	HUMAN PRESCRIPTION DRUG	Quinapril	Quinapril Hydrochloride	TABLET, FILM COATED	ORAL	20130429	N/A	ANDA	ANDA202725	Aurobindo Pharma Limited	QUINAPRIL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-617-30)
65862-617-78	65862-617	HUMAN PRESCRIPTION DRUG	Quinapril	Quinapril Hydrochloride	TABLET, FILM COATED	ORAL	20130429	N/A	ANDA	ANDA202725	Aurobindo Pharma Limited	QUINAPRIL HYDROCHLORIDE	5 mg/1	10 BLISTER PACK in 1 CARTON (65862-617-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-617-10)
65862-617-90	65862-617	HUMAN PRESCRIPTION DRUG	Quinapril	Quinapril Hydrochloride	TABLET, FILM COATED	ORAL	20130429	N/A	ANDA	ANDA202725	Aurobindo Pharma Limited	QUINAPRIL HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-617-90)
63629-7934-1	63629-7934	HUMAN PRESCRIPTION DRUG	Quinapril	Quinapril Hydrochloride	TABLET, FILM COATED	ORAL	20190301	N/A	ANDA	ANDA202725	Bryant Ranch Prepack	QUINAPRIL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-7934-1)