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=ANDA208465"
符合检索条件的记录共 9 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
50228-342-10 50228-342 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA208465 ScieGen Pharmaceuticals Inc HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (50228-342-10)
50228-342-30 50228-342 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA208465 ScieGen Pharmaceuticals Inc HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50228-342-30)
50228-342-90 50228-342 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA208465 ScieGen Pharmaceuticals Inc HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50228-342-90)
50228-343-10 50228-343 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA208465 ScieGen Pharmaceuticals Inc HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (50228-343-10)
50228-343-30 50228-343 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA208465 ScieGen Pharmaceuticals Inc HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50228-343-30)
50228-343-90 50228-343 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA208465 ScieGen Pharmaceuticals Inc HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50228-343-90)
50228-344-10 50228-344 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA208465 ScieGen Pharmaceuticals Inc HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (50228-344-10)
50228-344-30 50228-344 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA208465 ScieGen Pharmaceuticals Inc HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50228-344-30)
50228-344-90 50228-344 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA208465 ScieGen Pharmaceuticals Inc HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50228-344-90)
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