欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0425/002
药品名称Selenase oral solution 500 microgram
活性成分
    • [No Active-Substance specified] 0.0 -
剂型Oral solution
上市许可持有人Biosyn Arzneimittel GmbH Schorndorfer Strasse 32 D-70734 Fellbach Germany
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Portugal (PT)
    • Italy (IT)
    • Hungary (HU)
      Selenase bels. old.
    • Slovakia (SK)
      selenase perorálny roztok 500 µg
许可日期2003/11/01
最近更新日期2023/04/17
药物ATC编码
    • A12CE Selenium
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Bibliographic Article 4.8 (a) (ii)
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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