欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/2834/007
药品名称
Pregabalin EQL Pharma
活性成分
pregabalin 225.0 mg
剂型
Capsule, hard
上市许可持有人
EQL Pharma AB Stortorget 1 SE-222 23 Lund Sweden
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
Sweden (SE)
许可日期
2018/10/16
最近更新日期
2024/07/10
药物ATC编码
N03AX16 pregabalin
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
Common PIL Pregabalin_eql_pharma _ clean
Date of last change:2024/09/06
Final SPC
|
Common SmPC Pregabalin_eql_pharma _ clean
Date of last change:2024/09/06
Final Labelling
|
Final common labelling DK_H_2834_001_008_DC Pregabalin EQL Pharma
Date of last change:2024/09/06
市场状态
Positive
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