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

MR编号	NL/H/2284/001
药品名称	Propofol BioQ Pharma 10 mg/ml emulsion for injection/infusion
活性成分	propofol 10.0 mg/ml
剂型	Emulsion for injection or infusion
上市许可持有人	BioQ Pharma B.V. Prins Bernhardplein 200 1097 JB Amsterdam The Netherlands
参考成员国 - 产品名称	Netherlands (NL) Propofol Corden 10 mg/ml Emulsie voor injectie of infusie
互认成员国 - 产品名称	United Kingdom (Northern Ireland) (XI) Italy (IT)
许可日期	2012/05/01
最近更新日期	2023/08/03
药物ATC编码	N01AX10 propofol
申请类型	TypeLevel1：Abridged TypeLevel2：Multiple (Copy) 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 Labelling \| common labelDate of last change:2023/08/03 Final PL \| pl-propofol-bioq-10+20mg-20-07-clDate of last change:2020/10/30 Final SPC \| spc-propofol-bioq-10+20mg-20-09-clDate of last change:2020/10/30 PAR \| PAR_2284_DC_propofol_5 sept 2012Date of last change:2013/09/17 Final Product Information \| m1-3 Inner Labelling_Day 195_cleanDate of last change:2012/05/03 Final Product Information \| m1-3 Inner Labelling_Day 195_clean_2Date of last change:2012/05/03 Final Product Information \| m1-3 Outer Labelling_Day 195_cleanDate of last change:2012/05/03 Final Product Information \| m1-3 Outer Labelling_Day 195_clean_2Date of last change:2012/05/03 Final Product Information \| PIL_Day 210_clean_ AE added 120502Date of last change:2012/05/03 Final Product Information \| SPC_Day 210_clean_ AE added 120502Date of last change:2012/05/03
市场状态	Positive