欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号BE/H/0129/001
药品名称Dehydrobenzperidol 2,5mg/ml
活性成分
    • droperidol 2.5 mg/ml
剂型Solution for injection
上市许可持有人Kyowa Kirin Limited Galabank Business Park Galashields TD1 1QH United Kingdom
参考成员国 - 产品名称Belgium (BE)
Dehydrobenzperidol 2,5mg/ml oplossing voor injectie
互认成员国 - 产品名称
    • Netherlands (NL)
    • France (FR)
    • Sweden (SE)
    • Luxembourg (LU)
    • Denmark (DK)
      Xomolix
    • Iceland (IS)
      Dridol 2,5 mg/ml Stungulyf, lausn
    • United Kingdom (Northern Ireland) (XI)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Norway (NO)
    • Finland (FI)
    • Hungary (HU)
      XOMOLIX 2,5 mg/ml oldatos injekció
    • Slovenia (SI)
许可日期2007/09/27
最近更新日期2024/09/05
药物ATC编码
    • N01AX01 droperidol
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Biblio Art 10 a Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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