欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/1858/002
药品名称Sevikar HCT 40mg/5mg/12,5mg filmomhulde tabletten
活性成分
    • amlodipine besilate 5.0 mg
    • hydrochlorothiazide 12.5 mg
    • olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人Daiichi Sankyo Nederland B.V. Kabelweg 37 1014 BA Amsterdam The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Trivasc
互认成员国 - 产品名称
    • Germany (DE)
      TRIVASC 40 mg/5 mg/12,5 mg Filmtabletten
    • Belgium (BE)
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Spain (ES)
    • Italy (IT)
    • Greece (GR)
    • Romania (RO)
      Sevikar HCT 40 mg/5 mg/12,5 mg, comprimate filmate
许可日期2010/12/02
最近更新日期2024/09/04
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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