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
68180-413-06	68180-413	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130404	N/A	ANDA	ANDA201524	Lupin Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68180-413-06)
68180-413-09	68180-413	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130404	N/A	ANDA	ANDA201524	Lupin Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68180-413-09)
68180-414-06	68180-414	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130404	N/A	ANDA	ANDA201524	Lupin Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68180-414-06)
68180-414-09	68180-414	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130404	N/A	ANDA	ANDA201524	Lupin Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68180-414-09)