欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号AT/H/1310/001
药品名称Atorvastatin ratiopharm GmbH 10 mg film-coated tablets
活性成分
    • Atorvastatin calcium 10.0 mg
剂型Film-coated tablet
上市许可持有人Teva B.V. Sensweg 5, 2031GA Haarlem, Netherlands
参考成员国 - 产品名称Austria (AT)
互认成员国 - 产品名称
    • Slovakia (SK)
    • Italy (IT)
    • Croatia (HR)
    • Sweden (SE)
    • Norway (NO)
    • Germany (DE)
      Atorvastatin-ratiopharm 10 mg Filmtabletten
    • Finland (FI)
    • Denmark (DK)
      Atorvastatin ”Teva B.V.”
    • Poland (PL)
      Atorvastatin Teva B.V.
    • Belgium (BE)
      Atorvastatine Teva 10 mg filmomhulde tabletten
    • Latvia (LV)
    • Netherlands (NL)
    • Lithuania (LT)
      Atorvastatin TevaPharm 10 mg plėvele dengtos tabletės
    • Iceland (IS)
    • Estonia (EE)
    • Ireland (IE)
    • Hungary (HU)
      Atorvastatin-ratiopharm 10 mg filmtabletta
    • France (FR)
    • Bulgaria (BG)
    • Spain (ES)
    • Czechia (CZ)
      Atorvastatin ratiopharm
    • Portugal (PT)
许可日期2024/08/29
最近更新日期2025/01/03
药物ATC编码
    • C10AA05 atorvastatin
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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