欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
HU/H/0507/001
药品名称
Eliskardia
活性成分
Prasugrel 5.0 mg
剂型
Film-coated tablet
上市许可持有人
KRKA, d.d., Novo mesto Šmarješka cesta 6 8501 Novo mesto Slovenia
参考成员国 - 产品名称
Hungary (HU)
互认成员国 - 产品名称
Lithuania (LT)
Eliskardia 5 mg plėvele dengtos tabletės
Estonia (EE)
ELISKARDIA
Bulgaria (BG)
Eliscardia
Czechia (CZ)
Eliskardia
Romania (RO)
Slovenia (SI)
Eliskardia 5 mg filmsko obložene tablete
Croatia (HR)
Eliskardia 5 mg filmom obložene tablete
许可日期
2018/07/26
最近更新日期
2022/09/07
药物ATC编码
B01AC22 prasugrel
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
PubAR
|
EliskardiaPAReng
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase