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
33342-173-10	33342-173	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20230602	N/A	ANDA	ANDA204801	Macleods Pharmaceuticals Limited	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-173-10)
33342-173-12	33342-173	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20230602	N/A	ANDA	ANDA204801	Macleods Pharmaceuticals Limited	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	10 BLISTER PACK in 1 CARTON (33342-173-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
71335-3029-2	71335-3029	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20260205	N/A	ANDA	ANDA204801	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-3029-2)
71335-3030-2	71335-3030	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20260205	N/A	ANDA	ANDA204801	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-3030-2)
71335-3030-3	71335-3030	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20260205	N/A	ANDA	ANDA204801	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-3030-3)
71335-3031-1	71335-3031	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20260205	N/A	ANDA	ANDA204801	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-3031-1)
71335-3029-3	71335-3029	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20260205	N/A	ANDA	ANDA204801	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-3029-3)
71335-3030-1	71335-3030	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20260205	N/A	ANDA	ANDA204801	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-3030-1)
71335-3029-1	71335-3029	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20260205	N/A	ANDA	ANDA204801	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-3029-1)
71335-3031-2	71335-3031	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20260205	N/A	ANDA	ANDA204801	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-3031-2)
71335-3031-3	71335-3031	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20260205	N/A	ANDA	ANDA204801	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-3031-3)