欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1619/003
药品名称
Vardenafil Krka
活性成分
vardenafil hydrochloride 20.0 mg
剂型
Film-coated tablet
上市许可持有人
KRKA, d.d.Novo Mesto, Slovenia Šmarješka cesta 6, 8501
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Denmark (DK)
Belgium (BE)
Vardenafil Krka 20 mg filmomhulde tabletten
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Vardenafil Krka 20 mg Filmtabletten
France (FR)
Spain (ES)
Portugal (PT)
Italy (IT)
Norway (NO)
Vardenafil Krka
Finland (FI)
许可日期
2017/02/16
最近更新日期
2024/02/08
药物ATC编码
G04BE09 vardenafil
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Multiple (Copy) 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
PAR Summary
|
SE/H/1619/003_PAR Summary
Date of last change:2017/04/28
PAR
|
SE/H/1619/003_PAR
Date of last change:2017/04/28
Final PL
|
SE/H/1619/003_Final PL
Date of last change:2017/04/03
Final SPC
|
SE/H/1619/003_Final SPC
Date of last change:2017/04/03
市场状态
Positive
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