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
0024-5855-30	0024-5855	HUMAN PRESCRIPTION DRUG	Avalide	irbesartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130101	N/A	NDA	NDA020758	sanofi-aventis U.S. LLC	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0024-5855-30)
0024-5856-30	0024-5856	HUMAN PRESCRIPTION DRUG	Avalide	irbesartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130101	N/A	NDA	NDA020758	sanofi-aventis U.S. LLC	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0024-5856-30)
0955-1045-90	0955-1045	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	irbesartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190930	N/A	NDA AUTHORIZED GENERIC	NDA020758	Winthrop U.S, a business of sanofi-aventis U.S. LLC	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0955-1045-90)
0955-1046-90	0955-1046	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	irbesartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190930	N/A	NDA AUTHORIZED GENERIC	NDA020758	Winthrop U.S, a business of sanofi-aventis U.S. LLC	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0955-1046-90)