欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DK/H/0784/001
药品名称Sevofluran "Baxter"
活性成分
    • sevoflurane 1.0 ml/ml
剂型Inhalation vapour, liquid
上市许可持有人BAXTER A/S Tobaksvejen 23 A DK-2860 Søborg Denmark
参考成员国 - 产品名称Denmark (DK)
Sevofluran "Baxter"
互认成员国 - 产品名称
    • Germany (DE)
      Sevoflurane Baxter
    • Netherlands (NL)
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
      Sevofluran Baxter
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
      SEVOFLURANE BAXTER
    • Hungary (HU)
      SEVOFLURANE BAXTER folyadék inhalációs gőz képzéséhez
    • Belgium (BE)
    • Iceland (IS)
    • Ireland (IE)
    • Austria (AT)
      Sevofluran Baxter 100 % - Flüssigkeit zur Herstellung eines Dampfs zur Inhalation
    • Spain (ES)
    • Latvia (LV)
    • Lithuania (LT)
      Sevoflurane Baxter 100 % inhaliaciniai garai, skystis
    • Estonia (EE)
      SEVOFLURANE BAXTER 100%
    • Bulgaria (BG)
      Sevoflurane Baxter
    • Czechia (CZ)
      Sevoflurane Baxter
    • Romania (RO)
      SEVOFLURAN BAXTER 100% lichid pentru vapori de inhalat
    • Slovakia (SK)
      Sevoflurane Baxter
    • Slovenia (SI)
许可日期2005/08/01
最近更新日期2024/05/31
药物ATC编码
    • N01AB08 sevoflurane
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Initial Application
  • 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