欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/V/0384/001
药品名称Recudon
活性成分
    • fenpipramide hydrochloride 0.13 mg/ml
    • levomethadone hydrochloride 2.5 mg/ml
剂型Solution for injection
上市许可持有人Alfasan Nederland B.V. Kuipersweg 9 3449 JA Woerden The Netherlands
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Croatia (HR)
    • Finland (FI)
    • Belgium (BE)
      Recudon 2,5 mg/ml + 0,125 mg/ml
    • United Kingdom (Northern Ireland) (XI)
    • Poland (PL)
    • Luxembourg (LU)
    • Latvia (LV)
    • Iceland (IS)
    • Lithuania (LT)
    • Ireland (IE)
    • Estonia (EE)
    • Austria (AT)
    • Hungary (HU)
    • France (FR)
    • Bulgaria (BG)
    • Spain (ES)
    • Cyprus (CY)
    • Portugal (PT)
    • Czechia (CZ)
    • Italy (IT)
    • Romania (RO)
    • Greece (GR)
    • Slovakia (SK)
    • Sweden (SE)
    • Germany (DE)
    • Slovenia (SI)
    • Norway (NO)
    • Denmark (DK)
许可日期2023/05/31
最近更新日期2023/10/06
药物ATC编码
    • QN02AC52 methadone, combinations excl. psycholeptics
申请类型
  • TypeLevel1：food
  • TypeLevel2：Pharmaceutical
  • TypeLevel3：Generic - art 13.2 Dir 2001/82/EC
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
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    市场状态Positive
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