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
63187-943-60	63187-943	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180101	N/A	ANDA	ANDA201662	Proficient Rx LP	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 80 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-943-60)
63187-943-90	63187-943	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180101	N/A	ANDA	ANDA201662	Proficient Rx LP	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-943-90)
62332-080-10	62332-080	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160520	N/A	ANDA	ANDA201662	Alembic Pharmaceuticals Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	100 TABLET, FILM COATED in 1 CARTON (62332-080-10)
62332-080-30	62332-080	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160520	N/A	ANDA	ANDA201662	Alembic Pharmaceuticals Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-080-30)
62332-080-71	62332-080	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160520	N/A	ANDA	ANDA201662	Alembic Pharmaceuticals Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62332-080-71)
62332-080-90	62332-080	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160520	N/A	ANDA	ANDA201662	Alembic Pharmaceuticals Inc.	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-080-90)
46708-454-10	46708-454	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160520	N/A	ANDA	ANDA201662	Alembic Pharmaceuticals Limited	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	100 TABLET, FILM COATED in 1 CARTON (46708-454-10)
46708-454-30	46708-454	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160520	N/A	ANDA	ANDA201662	Alembic Pharmaceuticals Limited	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-454-30)
46708-454-71	46708-454	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160520	N/A	ANDA	ANDA201662	Alembic Pharmaceuticals Limited	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (46708-454-71)
46708-454-90	46708-454	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160520	N/A	ANDA	ANDA201662	Alembic Pharmaceuticals Limited	HYDROCHLOROTHIAZIDE; VALSARTAN	12.5 mg/1; 160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-454-90)
71335-0853-1	71335-0853	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA201662	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; VALSARTAN	25 mg/1; 320 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0853-1)
71335-0853-2	71335-0853	HUMAN PRESCRIPTION DRUG	Valsartan and Hydrochlorothiazide	Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA201662	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; VALSARTAN	25 mg/1; 320 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0853-2)