欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/4343/001
药品名称Abacavir/Lamivudin Teva 600 mg/300 mg Filmtabletten
活性成分
    • Abacavir 600.0 mg
    • Lamivudine 300.0 mg
剂型Film-coated tablet
上市许可持有人TEVA GmbH Graf-Arco-Str. 3 89079 Ulm Germany
参考成员国 - 产品名称Germany (DE)
Abacavir/Lamivudin Teva 600 mg/300 mg Filmtabletten
互认成员国 - 产品名称
    • Denmark (DK)
      Abacavir/Lamivudine "Teva"
    • Netherlands (NL)
    • Austria (AT)
      Abacavir/Lamivudin ratiopharm 600 mg/300 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Hungary (HU)
      ABACAVIR/LAMIVUDINE TEVA 600 mg/300 mg filmtabletta
    • Romania (RO)
    • Croatia (HR)
      Abakavir/lamivudin Pliva 600 mg/300 mg filmom obložene tablete
    • United Kingdom (Northern Ireland) (XI)
许可日期2016/04/29
最近更新日期2024/10/02
药物ATC编码
    • J05AR02 lamivudine and abacavir
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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