欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IT/H/0902/002
药品名称
DRULLUB
活性成分
Prasugrelhydrobromid 10.0 mg
剂型
Film-coated tablet
上市许可持有人
S.F. Group S.r.l. Via Tiburtina 1143 00156 Roma Italy
参考成员国 - 产品名称
Italy (IT)
互认成员国 - 产品名称
Netherlands (NL)
Drullub 10mg
许可日期
2018/02/09
最近更新日期
2024/03/08
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
Final Product Information
|
IT_H_0902_001_002_IB_004_G
Date of last change:2024/09/06
Final PL
|
common PIL prasugrel NL_H_3996_01_02 V1_1 171218_clean
Date of last change:2024/09/06
Final SPC
|
common SPC prasugrel NL_H_3996_01_02 V1_1 171218_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase