欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5434/002
药品名称Pirfenidon Vivanta 801 mg filmomhulde tabletten
活性成分
    • Pirfenidone 801.0 mg
剂型Film-coated tablet
上市许可持有人Vivanta Generics s.r.o. Trtinova 260/1 Cakovice 196 00 Prague Czechia
参考成员国 - 产品名称Netherlands (NL)
Pirfenidon Vivanta 801 mg filmomhulde tabletten
互认成员国 - 产品名称
    • Norway (NO)
    • Czech Republic (CZ)
      Pirfenidon MSN
    • Romania (RO)
    • Cyprus (CY)
      Pirfenidon MSN 801mg film-coated tablets
    • Slovak Republic (SK)
    • Ireland (IE)
    • Slovenia (SI)
    • Italy (IT)
    • Croatia (HR)
    • Poland (PL)
    • Germany (DE)
      Pirfenidon Vivanta 801 mg Filmtabletten
    • Latvia (LV)
    • Lithuania (LT)
      Pirfenidone MSN 801 mg plėvele dengtos tabletės
    • Spain (ES)
    • Estonia (EE)
    • Portugal (PT)
    • Hungary (HU)
      Pirfenidon MSN 801 mg filmtabletta
    • Sweden (SE)
    • Bulgaria (BG)
      Pirfenidone MSN
许可日期2022/06/22
最近更新日期2025/12/18
药物ATC编码
    • L04AX05 pirfenidone
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Other
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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