欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0692/002
药品名称Citalopram 20 PCH, film-omhulde tabletten 20 mg
活性成分
    • citalopram hydrobromide 20.0 mg
剂型Film-coated tablet
上市许可持有人Pharmachemie B.V. P.O. Box 552 2003 RN Haarlem The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Citalopram
互认成员国 - 产品名称
    • Iceland (IS)
      Oropram
    • Denmark (DK)
    • Belgium (BE)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Sweden (SE)
    • Norway (NO)
    • Latvia (LV)
    • Lithuania (LT)
      Citalopram -Teva 20 mg plėvele dengtos tabletės
    • Estonia (EE)
      CITALOPRAM - TEVA 20MG
    • Czechia (CZ)
    • Slovakia (SK)
许可日期2006/02/22
最近更新日期2024/04/09
药物ATC编码
    • N06AB04 citalopram
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Generic [Article 10.1.(a)(iii), first paragraph]
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
市场状态Positive
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase