欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DK/H/3253/002
药品名称Pirfenidone Accord 801 mg
活性成分
    • pirfenidone 801.0 mg
剂型Film-coated tablet
上市许可持有人Accord Healthcare B.V. Winthontlaan 200, 3526 KV Utrecht Netherlands
参考成员国 - 产品名称Denmark (DK)
Pirfenidone Accord
互认成员国 - 产品名称
    • Latvia (LV)
    • Lithuania (LT)
      Pirfenidone Accord 801 mg plėvele dengtos tabletės
    • Estonia (EE)
    • Germany (DE)
      Pirfenidone Accord 801 mg Filmtabletten
    • Croatia (HR)
    • Belgium (BE)
    • Netherlands (NL)
    • Cyprus (CY)
      Pirfenidone Accord 801 mg film-coated tablets.
    • Spain (ES)
    • Ireland (IE)
    • Czechia (CZ)
      Pirfenidone Accord
    • Italy (IT)
    • Austria (AT)
    • Slovenia (SI)
    • Sweden (SE)
    • France (FR)
    • Slovakia (SK)
    • Norway (NO)
    • Portugal (PT)
    • Finland (FI)
    • Greece (GR)
    • Poland (PL)
      Pirfenidone Accord
许可日期2022/07/07
最近更新日期2023/05/11
药物ATC编码
    • L04AX05 pirfenidone
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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