欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）

MR编号	SI/H/0166/002
药品名称	Tadagis 5 mg Film-coated tablets
活性成分	tadalafil 5.0 mg
剂型	Film-coated tablet
上市许可持有人	Krka, d.d., Novo mesto Šmarješka cesta 6 8501 Novo mesto Slovenia
参考成员国 - 产品名称	Slovenia (SI) Tadafin 5 mg filmsko obložene tablete
互认成员国 - 产品名称	Malta (MT) Germany (DE)
许可日期	2016/12/23
最近更新日期	2021/12/21
药物ATC编码	G04BE08 tadalafil
申请类型	TypeLevel1：Known Active Substance 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-track-1_corr_fin_clDate of last change:2019/08/23 Final Product Information \| common-combined-track-4_corr_fin_clDate of last change:2019/08/23 Final Product Information \| common-combined-track-2_corr_fin_clDate of last change:2019/08/23 Final Product Information \| common-combined-track-3_corr_fin_clDate of last change:2019/08/23
市场状态	Positive