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
31722-888-30	31722-888	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil and hydrochlorothiazide	Olmesartan medoxomil and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250725	N/A	ANDA	ANDA209199	Camber Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-888-30)
31722-888-32	31722-888	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil and hydrochlorothiazide	Olmesartan medoxomil and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250725	N/A	ANDA	ANDA209199	Camber Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	10 BLISTER PACK in 1 CARTON (31722-888-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK
31722-888-90	31722-888	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil and hydrochlorothiazide	Olmesartan medoxomil and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250725	N/A	ANDA	ANDA209199	Camber Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-888-90)
31722-887-30	31722-887	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil and hydrochlorothiazide	Olmesartan medoxomil and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250725	N/A	ANDA	ANDA209199	Camber Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-887-30)
31722-887-32	31722-887	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil and hydrochlorothiazide	Olmesartan medoxomil and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250725	N/A	ANDA	ANDA209199	Camber Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	10 BLISTER PACK in 1 CARTON (31722-887-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK
31722-887-90	31722-887	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil and hydrochlorothiazide	Olmesartan medoxomil and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250725	N/A	ANDA	ANDA209199	Camber Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-887-90)
31722-886-30	31722-886	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil and hydrochlorothiazide	Olmesartan medoxomil and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250725	N/A	ANDA	ANDA209199	Camber Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-886-30)
31722-886-32	31722-886	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil and hydrochlorothiazide	Olmesartan medoxomil and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250725	N/A	ANDA	ANDA209199	Camber Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	10 BLISTER PACK in 1 CARTON (31722-886-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK
31722-886-90	31722-886	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil and hydrochlorothiazide	Olmesartan medoxomil and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250725	N/A	ANDA	ANDA209199	Camber Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-886-90)