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
42291-924-90	42291-924	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230727	N/A	NDA	NDA021532	AvKARE	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42291-924-90)
42291-925-90	42291-925	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230727	N/A	NDA	NDA021532	AvKARE	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42291-925-90)
42291-926-90	42291-926	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230727	N/A	NDA	NDA021532	AvKARE	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42291-926-90)
0713-0863-30	0713-0863	HUMAN PRESCRIPTION DRUG	Benicar HCT	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220901	N/A	NDA	NDA021532	Cosette Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0863-30)
0713-0864-30	0713-0864	HUMAN PRESCRIPTION DRUG	Benicar HCT	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220901	N/A	NDA	NDA021532	Cosette Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0864-30)
0713-0865-30	0713-0865	HUMAN PRESCRIPTION DRUG	Benicar HCT	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220901	N/A	NDA	NDA021532	Cosette Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0865-30)