欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0610/001
药品名称
Scandonest
活性成分
mepivacaine 30.0 mg/ml
剂型
Solution for injection
上市许可持有人
Septodont France
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Germany (DE)
Denmark (DK)
Belgium (BE)
Netherlands (NL)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
France (FR)
Italy (IT)
Greece (GR)
Norway (NO)
Poland (PL)
Latvia (LV)
Lithuania (LT)
Estonia (EE)
Hungary (HU)
Bulgaria (BG)
Romania (RO)
Slovakia (SK)
Slovenia (SI)
Spain (ES)
Portugal (PT)
Finland (FI)
Czechia (CZ)
Scandonest 30 mg/ml, injekční roztok
Croatia (HR)
许可日期
2007/05/08
最近更新日期
2024/08/07
药物ATC编码
N01BB03 mepivacaine
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
附件文件下载
Final PL
|
SE_H_0610_001_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_0610_001_Final SPC
Date of last change:2024/09/06
市场状态
Positive
©2006-2024
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European Union HMA Authorisation of Medicines DataBase