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

MR编号	NL/H/1925/003
药品名称	Sildenafil CF 50 mg, filmomhulde tabletten
活性成分	sildenafil citrate 50.0 mg
剂型	Film-coated tablet
上市许可持有人	Centrafarm B.V. Van de Reijtstraat 31-E 4814 NE Breda Nederland
参考成员国 - 产品名称	Netherlands (NL) Sildenafil CF 50 mg, filmomhulde tabletten
互认成员国 - 产品名称	Iceland (IS) Sildenafil CF 50 mg, filmomhulde tabletten Germany (DE) Sildivilb 50 mg Filmtabletten Denmark (DK) Belgium (BE) Luxembourg (LU) Ireland (IE) France (FR) Sweden (SE) Sildenafil STADA Finland (FI)
许可日期	2010/12/16
最近更新日期	2023/04/06
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 SPC \| 1_3_1_SmPC_common_en_NL1925_V020_clDate of last change:2022/08/11 Final Product Information \| 1.3.1-SmPC-Sildenafil_NL-H-1925_20200624_PH-clDate of last change:2020/08/20 Final Product Information \| 1.3.1-LAB-outer-common-en-NL1925-V16d27-clDate of last change:2020/08/20 Final Product Information \| 1.3.1-PL-Sildenafil_NL-H-1925_20200624_PH-clDate of last change:2020/08/20 Final PL \| 1.3.1-PIL-common-en-NL1925-V013-clDate of last change:2019/08/23 Final PL \| 1.3.1-SPC-common-en-NL1925-V013-clDate of last change:2019/08/23 Final Labelling \| EOP-Lab_inner_Sildenafil-1925-26_25mg_50mg_100mg_cl.eanDate of last change:2011/04/07 Final Labelling \| EOP-Lab_outer_Sildenafil-1925-26_25mg_50mg_100mg_cleanDate of last change:2011/04/07
市场状态	Positive