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
65862-550-05	65862-550	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; 320 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-550-05)
65862-550-90	65862-550	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; 320 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-550-90)
63187-312-30	63187-312	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA202519	Proficient Rx LP	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-312-30)
63187-312-90	63187-312	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA202519	Proficient Rx LP	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-312-90)