欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1646/003
药品名称
Tadalafil Zentiva
活性成分
Tadalafil 20.0 mg
剂型
Film-coated tablet
上市许可持有人
Zentiva k.s. Czech Republic
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Italy (IT)
Germany (DE)
Tadalafil Zentiva 20 mg Filmtabletten
Spain (ES)
Latvia (LV)
Lithuania (LT)
Tadalafil Zentiva 20 mg plėvele dengtos tabletės
Portugal (PT)
Estonia (EE)
Czechia (CZ)
Tadalafil Zentiva
许可日期
2017/05/24
最近更新日期
2024/09/09
药物ATC编码
G04BE08 tadalafil
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
|
SE_H_1646_003_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_1646_003_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_1646_003_PAR
Date of last change:2024/09/06
PubAR Summary
|
SE_H_1646_003_PAR Summary
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase