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

MR编号	SI/H/0164/004
药品名称	Tadalafil Krka 20 mg Film-coated tablets
活性成分	tadalafil 20.0 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) Tadalafil Krka 20 mg filmsko obložene tablete
互认成员国 - 产品名称	Denmark (DK) Belgium (BE) Iceland (IS) United Kingdom (Northern Ireland) (XI) Ireland (IE) Austria (AT) France (FR) Spain (ES) Portugal (PT) Italy (IT) Sweden (SE) Norway (NO) Finland (FI)
许可日期	2017/02/21
最近更新日期	2021/12/20
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-1Date of last change:2017/12/20 Final Product Information \| common-combined-track-2Date of last change:2017/12/20 Final Product Information \| common-combined-track-3Date of last change:2017/12/20 Final Product Information \| common-combined-track-4Date of last change:2017/12/20
市场状态	Positive