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
29300-215-19	29300-215	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180331	N/A	ANDA	ANDA207018	Unichem Pharmaceuticals (USA), Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-215-19)
29300-216-10	29300-216	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180331	N/A	ANDA	ANDA207018	Unichem Pharmaceuticals (USA), Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-216-10)
29300-216-13	29300-216	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180331	N/A	ANDA	ANDA207018	Unichem Pharmaceuticals (USA), Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-216-13)
29300-216-19	29300-216	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180331	N/A	ANDA	ANDA207018	Unichem Pharmaceuticals (USA), Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-216-19)
29300-215-13	29300-215	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180331	N/A	ANDA	ANDA207018	Unichem Pharmaceuticals (USA), Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-215-13)
29300-215-10	29300-215	HUMAN PRESCRIPTION DRUG	Irbesartan and Hydrochlorothiazide	Irbesartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20180331	N/A	ANDA	ANDA207018	Unichem Pharmaceuticals (USA), Inc.	HYDROCHLOROTHIAZIDE; IRBESARTAN	12.5 mg/1; 150 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-215-10)