欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FR/H/0426/003
药品名称
Sildenafil Mylan 100mg, film-coated tablet
活性成分
sildenafil citrate 100.0 mg
剂型
Film-coated tablet
上市许可持有人
Mylan
参考成员国 - 产品名称
France (FR)
互认成员国 - 产品名称
Germany (DE)
Sildenafil Mylan 100 mg Filmtabletten
Denmark (DK)
Netherlands (NL)
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Norway (NO)
Hungary (HU)
SILDENAFIL MYLAN 100 mg filmtabletta
Czechia (CZ)
Sildenafil Mylan 100 mg potahované tablety
Slovakia (SK)
Sildenafil Mylan 100 mg
Belgium (BE)
Sildenafil Viatris 100 mg FC tablets
Luxembourg (LU)
Cyprus (CY)
SILDENAFIL MYLAN TABLET, FILM COATED 100MG
Malta (MT)
许可日期
2010/08/02
最近更新日期
2024/02/19
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 Product Information
|
common_combined_h_0426_clean
Date of last change:2022/07/22
Final SPC
|
Sildenafil Mylan - FR 426 IB - D30 Approval
Date of last change:2013/04/19
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase