欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/1113/003
药品名称Sevikar 40 mg/10 mg
活性成分
    • amlodipine 10.0 mg
    • olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人Daiichi Sankyo Europe GmbH München Germany
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Romania (RO)
      SEVIKAR 40 mg/10 mg comprimate filmate
    • Germany (DE)
      Sevikar 40 mg/10 mg Filmtabletten
    • Belgium (BE)
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
      Sevikar
    • Italy (IT)
    • Greece (GR)
许可日期2008/07/30
最近更新日期2024/08/22
药物ATC编码
    • C09D ANGIOTENSIN II RECEPTOR BLOCKERS (ARBs), COMBINATIONS
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Fixed combination Art 10b Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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