欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3651/006
药品名称Darunavir Sandoz 800 mg, filmcoated tablets
活性成分
    • DARUNAVIR 800.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Hospitaaldreef 29 1315 RC Almere Nederland
参考成员国 - 产品名称Netherlands (NL)
Darunavir Sandoz 800 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Romania (RO)
      Darunavir Sandoz 800 mg comprimate filmate
    • Croatia (HR)
      Darunavir Sandoz 800 mg filmom obložene tablete
    • United Kingdom (Northern Ireland) (XI)
    • Denmark (DK)
    • Austria (AT)
    • Ireland (IE)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Sweden (SE)
    • Finland (FI)
    • Poland (PL)
      Darunavir Sandoz
    • Estonia (EE)
许可日期2017/02/15
最近更新日期2024/08/30
药物ATC编码
    • J05AE10 darunavir
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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