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
71205-249-90	71205-249	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190401	N/A	ANDA	ANDA078946	Proficient Rx LP	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-249-90)
71205-249-60	71205-249	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190401	N/A	ANDA	ANDA078946	Proficient Rx LP	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 80 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-249-60)
71205-249-30	71205-249	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190401	N/A	ANDA	ANDA078946	Proficient Rx LP	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-249-30)
53002-1784-9	53002-1784	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190601	N/A	ANDA	ANDA078946	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (53002-1784-9)
53002-1787-3	53002-1787	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190601	N/A	ANDA	ANDA078946	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 320 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-1787-3)
53002-1787-9	53002-1787	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190601	N/A	ANDA	ANDA078946	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 320 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (53002-1787-9)
53002-1788-3	53002-1788	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190601	N/A	ANDA	ANDA078946	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	25 mg/1; 320 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-1788-3)
53002-1788-9	53002-1788	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190601	N/A	ANDA	ANDA078946	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	25 mg/1; 320 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (53002-1788-9)
53002-1784-3	53002-1784	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190601	N/A	ANDA	ANDA078946	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-1784-3)
53002-1785-3	53002-1785	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190601	N/A	ANDA	ANDA078946	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	25 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-1785-3)
53002-1785-9	53002-1785	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190601	N/A	ANDA	ANDA078946	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	25 mg/1; 160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (53002-1785-9)