欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SI/H/0266/001
药品名称Tigecycline AptaPharma 50 mg powder for solution for infusion
活性成分
    • TIGECYCLINE 50.0 mg
剂型Powder for solution for infusion
上市许可持有人Apta Medica Internacional Družba Za Trženje Farmacevtskih Izdelkov In Medicinskih Pripomočkov d.o.o. Likozarjeva Ulica 6, 1000 Ljubljana, Slovenia
参考成员国 - 产品名称Slovenia (SI)
Tigeciklin AptaPharma 50 mg prašek za raztopino za infundiranje
互认成员国 - 产品名称
    • Czechia (CZ)
      Tigecycline AptaPharma
    • Romania (RO)
      Tigeciclină AptaPharma 50 mg pulbere pentru soluție perfuzabilă
    • Slovakia (SK)
    • Malta (MT)
      Tigecycline AptaPharma 50 mg powder for solution for infusion
    • Croatia (HR)
    • Austria (AT)
    • Poland (PL)
      Tigecycline AptaPharm
    • Hungary (HU)
    • Bulgaria (BG)
      Tigecycline AptaPharma
    • Cyprus (CY)
      Tigecycline AptaPharma 50 mg κόνις για διάλυμα προς έγχυση
许可日期2024/03/07
最近更新日期2024/03/07
药物ATC编码
    • J01AA12 tigecycline
申请类型
  • TypeLevel1:Known Active Substance
  • 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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