欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IE/H/1149/001
药品名称
Prasugrel Krka
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
Ireland (IE)
互认成员国 - 产品名称
Denmark (DK)
Belgium (BE)
Prasugrel Krka 5 mg filmomhulde tabletten
Iceland (IS)
Prasugrel Krka 5 mg Filmuhúðuð tafla
United Kingdom (Northern Ireland) (XI)
Austria (AT)
Prasugrel HCS 5 mg Filmtabletten
Italy (IT)
Sweden (SE)
Norway (NO)
Prasugrel Krka
许可日期
2018/07/26
最近更新日期
2024/02/19
药物ATC编码
B01AC22 prasugrel
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
PubAR
|
PrasugelKrkaPAReng
Date of last change:2024/09/06
PubAR
|
Public_AR_PA1347_080_001_02032022125350
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase