欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5921/001
药品名称Amlodipine (als besilaat) Teva 5 mg, tablets
活性成分
    • AMLODIPINE BESILATE 5.0 mg
剂型Tablet
上市许可持有人Teva B.V. Swensweg 5 2031 GA Haarlem The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Amlodipine (als besilaat) Teva 5 mg, tabletten
互认成员国 - 产品名称
    • Iceland (IS)
    • Ireland (IE)
    • Austria (AT)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Bulgaria (BG)
      Amlovask 5mg tablets
    • Norway (NO)
    • Czech Republic (CZ)
      Amlodipin Teva
    • Finland (FI)
    • Slovak Republic (SK)
    • Germany (DE)
      Amlodipin-ratiopharm 5 mg Tabletten
    • Estonia (EE)
    • Croatia (HR)
    • Denmark (DK)
      Amlodipin ”Teva B.V.”
    • Hungary (HU)
      Amlodipin Teva GmbH 5-10 mg tabletta
    • Belgium (BE)
      Amlodipine Teva Generics 5 mg tabletten
许可日期2025/10/28
最近更新日期2025/11/19
药物ATC编码
    • C08CA01 amlodipine
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
    市场状态Positive
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