欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5171/002
药品名称Teicoplanin Sun 400 mg powder and solvent for infusion/injection or oral solution
活性成分
    • teicoplanin 400.0 mg
剂型Powder and solvent for solution for injection/infusion
上市许可持有人SUN pharmaceutical industries Europe B.V.
参考成员国 - 产品名称Netherlands (NL)
Teicoplanine SUN
互认成员国 - 产品名称
    • Italy (IT)
    • United Kingdom (Northern Ireland) (XI)
许可日期2021/08/11
最近更新日期2024/10/09
药物ATC编码
    • J01XA02 teicoplanin
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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