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
72205-148-30	72205-148	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250930	N/A	ANDA	ANDA217398	Novadoz Pharmaceuticals LLC	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72205-148-30)
72205-148-90	72205-148	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250930	N/A	ANDA	ANDA217398	Novadoz Pharmaceuticals LLC	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72205-148-90)
72205-148-99	72205-148	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250930	N/A	ANDA	ANDA217398	Novadoz Pharmaceuticals LLC	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72205-148-99)
72205-149-30	72205-149	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250930	N/A	ANDA	ANDA217398	Novadoz Pharmaceuticals LLC	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72205-149-30)
72205-149-90	72205-149	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250930	N/A	ANDA	ANDA217398	Novadoz Pharmaceuticals LLC	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72205-149-90)
72205-149-99	72205-149	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250930	N/A	ANDA	ANDA217398	Novadoz Pharmaceuticals LLC	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72205-149-99)
72205-147-30	72205-147	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250930	N/A	ANDA	ANDA217398	Novadoz Pharmaceuticals LLC	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72205-147-30)
72205-147-90	72205-147	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250930	N/A	ANDA	ANDA217398	Novadoz Pharmaceuticals LLC	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72205-147-90)
72205-147-99	72205-147	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil-hydrochlorothiazide	olmesartan medoxomil-hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250930	N/A	ANDA	ANDA217398	Novadoz Pharmaceuticals LLC	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72205-147-99)