欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1317/001
药品名称
Pregabalina Pentafarma Especialidades
活性成分
pregabalin 75.0 mg
剂型
Capsule, hard
上市许可持有人
Pentafarma Especialidades, Lda.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Czechia (CZ)
Pregabalin Pentafarma Especialidades 75 mg
许可日期
2015/04/14
最近更新日期
2024/08/28
药物ATC编码
N03AX16 pregabalin
申请类型
TypeLevel1:
Abridged
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
Final PL
|
1317_pil_proposed_75 mg_150mg_clean
Date of last change:2024/09/06
Final SPC
|
1317_smpc_proposed_75mg_150mg_clean
Date of last change:2024/09/06
PubAR
|
586881_586882_20151218_PAR_IRS
Date of last change:2024/09/06
Final Product Information
|
Immediate packaging_clean
Date of last change:2024/09/06
Final Product Information
|
Outer_packaging_clean
Date of last change:2024/09/06
Final Product Information
|
package_leaflet_clean
Date of last change:2024/09/06
Final Product Information
|
smpc_caps_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase