欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/2608/002
药品名称Leflunomid - 1A Pharma 20 mg Filmtabletten
活性成分
    • Leflunomide 20.0 mg
剂型Film-coated tablet
上市许可持有人1 A Pharma GmbH Keltenring 1 + 3 82041 Oberhaching Germany
参考成员国 - 产品名称Germany (DE)
Leflunomid Sandoz 20 mg Filmtabletten
互认成员国 - 产品名称
    • Belgium (BE)
    • Netherlands (NL)
    • United Kingdom (Northern Ireland) (XI)
    • Italy (IT)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
      Leflunomide Sandoz 20mg plėvele dengtos tabletės
    • Hungary (HU)
      LEFLUNOMID SANDOZ 20 mg filmtabletta
    • Czechia (CZ)
      Leflunomid Sandoz 20 mg, potahované tablety
    • Romania (RO)
      Leflunomidă Sandoz 20 mg, comprimate filmate
许可日期2010/10/11
最近更新日期2025/01/28
药物ATC编码
    • L04AA13 leflunomide
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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