欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号EE/H/0106/002
药品名称Donepezil Actavis
活性成分
    • Donepezil hydrochloride 10.0 mg
剂型Film-coated tablet
上市许可持有人Splitting: to PT/H/2023/001-002/ (CMS:ES) and IE/H/0500/001-002 (CMS: UK) Teva B.V. Swensweg 5 2031 GA Haarlem Netherlands
参考成员国 - 产品名称Estonia (EE)
Donepezil Actavis
互认成员国 - 产品名称
    • Norway (NO)
    • Poland (PL)
      Donecept
    • Lithuania (LT)
      Donepezil Actavis 10mg plėvele dengtos tabletės
    • Czechia (CZ)
    • Romania (RO)
      Donecept 10 mg, comprimate filmate
    • Iceland (IS)
    • Austria (AT)
      Donepezil Actavis 10 mg Filmtabletten
    • Sweden (SE)
许可日期2008/09/16
最近更新日期2024/10/02
药物ATC编码
    • N06DA02 donepezil
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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