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=ANDA207037"
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
67877-451-30 67877-451 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA207037 Ascend Laboratories, LLC HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67877-451-30)
67877-451-90 67877-451 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA207037 Ascend Laboratories, LLC HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (67877-451-90)
67877-453-30 67877-453 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA207037 Ascend Laboratories, LLC HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67877-453-30)
67877-453-90 67877-453 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA207037 Ascend Laboratories, LLC HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (67877-453-90)
67877-452-30 67877-452 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA207037 Ascend Laboratories, LLC HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67877-452-30)
67877-452-90 67877-452 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA207037 Ascend Laboratories, LLC HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (67877-452-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase