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
63187-981-30	63187-981	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180201	N/A	ANDA	ANDA077369	Proficient Rx LP	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-981-30)
63187-981-60	63187-981	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180201	N/A	ANDA	ANDA077369	Proficient Rx LP	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-981-60)
63187-981-90	63187-981	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180201	N/A	ANDA	ANDA077369	Proficient Rx LP	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-981-90)
70518-2247-0	70518-2247	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA077369	REMEDYREPACK INC.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2247-0)
70518-2619-0	70518-2619	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20200309	N/A	ANDA	ANDA077369	REMEDYREPACK INC.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2619-0)
0093-8232-56	0093-8232	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130827	N/A	ANDA	ANDA077369	Teva Pharmaceuticals USA, Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-8232-56)
0093-8232-98	0093-8232	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130827	N/A	ANDA	ANDA077369	Teva Pharmaceuticals USA, Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0093-8232-98)
0093-8238-56	0093-8238	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130124	N/A	ANDA	ANDA077369	Teva Pharmaceuticals USA, Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-8238-56)
0093-8238-98	0093-8238	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20130220	N/A	ANDA	ANDA077369	Teva Pharmaceuticals USA, Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0093-8238-98)
71335-1097-1	71335-1097	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190212	N/A	ANDA	ANDA077369	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1097-1)
71335-1097-2	71335-1097	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210317	N/A	ANDA	ANDA077369	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1097-2)
71335-1097-3	71335-1097	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220408	N/A	ANDA	ANDA077369	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-1097-3)
72162-1035-9	72162-1035	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230508	N/A	ANDA	ANDA077369	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72162-1035-9)