欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0611/003
药品名称
Sildenafil Bluefish
活性成分
sildenafil citrate 100.0 mg
剂型
Film-coated tablet
上市许可持有人
Bluefish Pharmaceuticals AB
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Poland (PL)
Sildenafil Bluefish
Iceland (IS)
许可日期
2012/04/03
最近更新日期
2024/06/05
药物ATC编码
G04BE03 sildenafil
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
|
Sildenafil Bluefish _PIL_clean_en
Date of last change:2024/09/06
Final SPC
|
Sildenafil Bluefish _SPC_clean_en
Date of last change:2024/09/06
Final Labelling
|
Sildenafil Bluefish_outer_100mg_clean_en
Date of last change:2024/09/06
Final Labelling
|
Sildenafil Bluefish_outer_25mg_clean_en
Date of last change:2024/09/06
Final Labelling
|
Sildenafil Bluefish_outer_50mg_clean_en
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase