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
65862-551-90	65862-551	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130321	N/A	ANDA	ANDA202519	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; VALSARTAN	25 mg/1; 320 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-551-90)
65862-547-99	65862-547	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130321	N/A	ANDA	ANDA202519	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 80 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-547-99)
65862-547-90	65862-547	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130321	N/A	ANDA	ANDA202519	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-547-90)
65862-548-10	65862-548	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130321	N/A	ANDA	ANDA202519	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	10 BLISTER PACK in 1 CARTON (65862-548-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK