欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SI/H/0226/001
药品名称Teicoplanin AptaPharma 200 mg powder and solvent for solution for injection/infusion
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Apta Medica Internacional d.o.o. Likozarjeva Ulica 6 1000 Ljubljana Slovenia
参考成员国 - 产品名称Slovenia (SI)
Teikoplanin AptaPharma 200 mg prašek in vehikel za raztopino za injiciranje ali infundiranje ali za peroralno suspenzijo
互认成员国 - 产品名称
    • Croatia (HR)
    • Austria (AT)
    • Poland (PL)
      Teicoplanin AptaPharma
    • Hungary (HU)
      Teicoplanin AptaPharma 200 mg por és oldószer oldatos injekcióhoz/infúzióhoz vagy belsőleges oldathoz
    • Bulgaria (BG)
      Teicoplanin AptaPharma
    • Cyprus (CY)
      Teicoplanin AptaPharma 200 mg powder and solvent for solution for injection/infusion
    • Czechia (CZ)
      Teicoplanin AptaPharma
    • Romania (RO)
      Teicoplanină AptaPharma 200 mg pulbere şi solvent pentru soluţie injectabilă/perfuzabilă sau soluţie orală
    • Slovakia (SK)
    • Malta (MT)
许可日期2022/02/03
最近更新日期2023/12/12
药物ATC编码
    • J01XA02 teicoplanin
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • 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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