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）
检索条件:" 注册申请号=ANDA204801"
符合检索条件的记录共 31 条，共 2 页，当前第 1 页 ，可点击列名称排序
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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
50090-7571-0 50090-7571 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20250605 N/A ANDA ANDA204801 A-S Medication Solutions HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7571-0)
33342-174-07 33342-174 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; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (33342-174-07)
33342-174-10 33342-174 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; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (33342-174-10)
33342-174-12 33342-174 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; 40 mg/1 10 BLISTER PACK in 1 CARTON (33342-174-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
33342-174-44 33342-174 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; 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (33342-174-44)
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)
71335-3031-2 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)
33342-173-07 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 30 TABLET, FILM COATED in 1 BOTTLE (33342-173-07)
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
33342-173-44 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 1000 TABLET, FILM COATED in 1 BOTTLE (33342-173-44)
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)
71335-3030-2 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)
72603-292-01 72603-292 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20240408 N/A ANDA ANDA204801 NorthStar RxLLC HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72603-292-01)
72603-292-02 72603-292 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20240408 N/A ANDA ANDA204801 NorthStar RxLLC HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72603-292-02)
70518-4517-0 70518-4517 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20251110 N/A ANDA ANDA204801 REMEDYREPACK INC. HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4517-0)
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)
71335-3029-2 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)
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