欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/2900/001
药品名称Brinzolamide Sandoz 10 mg/ml, oogdruppels, suspensie
活性成分
    • Brinzolamide 10.0 mg/ml
剂型Eye drops, suspension
上市许可持有人Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Brinzolamide Sandoz 10 mg/ml, oogdruppels, suspensie
互认成员国 - 产品名称
    • Latvia (LV)
      Brinzolamide Sandoz 10 mg/ml acu pilieni, suspensija
    • Estonia (EE)
      BRINZOLAMIDE SANDOZ
    • Germany (DE)
      Brinzolamid HEXAL 10 mg/ml Augentropfensuspension
    • Denmark (DK)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • France (FR)
    • Italy (IT)
    • Sweden (SE)
许可日期2014/05/25
最近更新日期2025/09/01
药物ATC编码
    • S01EC04 brinzolamide
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Initial Application
  • TypeLevel3：Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
附件文件下载
市场状态Positive
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase