欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号UK/H/6637/001
药品名称Teicoplanin 200 mg, powder and solvent for solution for injection/infusion or oral solution
活性成分
    • Teicoplanin 200.0 mg
剂型Powder and solvent for solution for injection/infusion
上市许可持有人Sun Pharmaceutical Industries Europe B.V. Polarisavenue 87 Hoofddorp 2132JH Netherlands
参考成员国 - 产品名称United Kingdom (UK)
互认成员国 - 产品名称
    • France (FR)
    • Germany (DE)
      Teicoplanin SUN 200 mg Pulver und Lösungsmittel zur Herstellung einer Injektions- und Infusionslösung
    • Italy (IT)
    • Spain (ES)
许可日期2019/02/15
最近更新日期2019/02/15
药物ATC编码
    • J01XA02 teicoplanin
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Initial Application
  • TypeLevel3：Generic
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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