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
65862-629-30	65862-629	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130222	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-629-30)
65862-629-90	65862-629	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130222	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-629-90)
65862-629-99	65862-629	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130222	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-629-99)
65862-630-05	65862-630	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130222	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-630-05)
65862-630-30	65862-630	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130222	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-630-30)
65862-630-90	65862-630	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130222	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-630-90)
65862-630-99	65862-630	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130222	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-630-99)
65862-631-90	65862-631	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160331	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	25 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-631-90)
65862-631-99	65862-631	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160331	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	25 mg/1; 300 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-631-99)
65862-631-30	65862-631	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160331	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	25 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-631-30)
65862-631-05	65862-631	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160331	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	25 mg/1; 300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-631-05)
65862-629-05	65862-629	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130222	N/A	ANDA	ANDA203630	Aurobindo Pharma Limited	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-629-05)