欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/0114/001
药品名称Teveten 200 mg
活性成分
    • eprosartan mesylate 200.0 mg
剂型Film-coated tablet
上市许可持有人SmithKline Beecham Pharma GmbH Leopoldstr. 175 D-80804 Muenchen
参考成员国 - 产品名称Germany (DE)
互认成员国 - 产品名称
    • Denmark (DK)
      Teveten 200 mg
    • Belgium (BE)
      Teveten 200 mg
    • Netherlands (NL)
      Teveten 200 mg
    • Luxembourg (LU)
      Teveten-200
    • Ireland (IE)
      Teveten 200 mg
    • Austria (AT)
      Teveten 200mg - Filmtabletten
    • France (FR)
      withdrawn from FR
    • Spain (ES)
      Tevetenz 200 mg
    • Portugal (PT)
      TEVETENZ
    • Italy (IT)
      TEVETENZ
    • Greece (GR)
      Teveten 200 mg
    • Sweden (SE)
      Teveten
    • Finland (FI)
      Teveten 200 mg
许可日期2001/12/13
最近更新日期2012/08/09
药物ATC编码
    • A ALIMENTARY TRACT AND METABOLISM
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：Full Dossier Article 4.8 Di 65/65
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
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