欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FR/H/0290/001
药品名称
Plasmion
活性成分
Sodium chloride 3.0 %
剂型
Solution for infusion
上市许可持有人
Fresenius Kabi France
参考成员国 - 产品名称
France (FR)
互认成员国 - 产品名称
Hungary (HU)
GELOPLASMA oldatos infúzió
Romania (RO)
Slovenia (SI)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Geloplasma Infusionslösung
Spain (ES)
Portugal (PT)
Italy (IT)
Poland (PL)
GELOPLASMA
Latvia (LV)
Geloplasma solution for infusion
Lithuania (LT)
GELOPLASMA infuzinis tirpalas
Estonia (EE)
GELOPLASMA
Czechia (CZ)
Geloplasma
Slovakia (SK)
GELOPLASMA
许可日期
2006/04/12
最近更新日期
2025/02/13
药物ATC编码
A ALIMENTARY TRACT AND METABOLISM
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Biblio Art 10 a Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
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市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase