欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IE/H/1149/002
药品名称
Prasugrel Krka
活性成分
Prasugrel 10.0 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 10 mg filmomhulde tabletten
Iceland (IS)
Prasugrel Krka 10 mg Filmuhúðuð tafla
United Kingdom (Northern Ireland) (XI)
Austria (AT)
Prasugrel HCS 10 mg Filmtabletten
France (FR)
Spain (ES)
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_002_02032022125347
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase