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

MR编号	NL/H/1823/002
药品名称	Sildenafil Accord
活性成分	sildenafil citrate 50.0 mg
剂型	Film-coated tablet
上市许可持有人	Accord Healthcare B.V. Winthontlaan 200, 3526 KV Utrecht, The Netherlands
参考成员国 - 产品名称	Netherlands (NL) Sildenafil Accord
互认成员国 - 产品名称	Ireland (IE) Denmark (DK) United Kingdom (Northern Ireland) (XI) France (FR) Italy (IT) Sweden (SE) Sildenafil Accord Latvia (LV) Lithuania (LT) Sildenafil Accord 50 mg plėvele dengtos tabletės Estonia (EE) SILDENAFIL ACCORD 50 MG
许可日期	2011/01/20
最近更新日期	2024/01/27
药物ATC编码	G04BE03 sildenafil
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 \| common_pl_cleanDate of last change:2022/09/13 Final SPC \| common_spc_cleanDate of last change:2022/09/13 Final Product Information \| common-pl-cleanDate of last change:2020/12/31 Final Product Information \| common-spc-trackchangeDate of last change:2020/12/31 Final Product Information \| common-pl-trackchangeDate of last change:2020/12/31 Final Product Information \| common-spc-cleanDate of last change:2020/12/31 Final Labelling \| common-combined-commonoutercleanDate of last change:2018/07/17 PAR \| PAR_1823_DC_sildenafil_20 apr 2011Date of last change:2014/02/19
市场状态	Positive