欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/2027/001
药品名称
Vimetso
活性成分
Metformin hydrochloride 850.0 mg
vildagliptin 50.0 mg
剂型
Film-coated tablet
上市许可持有人
Krka d.d. Novo Mesto, Slovenia
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Hungary (HU)
Glypvicombi 50 mg/850 mg -50 mg/1000 mgfilmtabletta
Bulgaria (BG)
Glypvicombi
Cyprus (CY)
Glypvicombi 50mg/850mg FCT
Czechia (CZ)
Glypvicombi 50mg/850mg potahované tablety
Slovakia (SK)
Vimetso 50 mg/850 mg filmom obalené tablety
Slovenia (SI)
Malta (MT)
Vimetso 50 mg/850 mg film-coated tablets
Greece (GR)
Croatia (HR)
Vimetso 50 mg/850 mg filmom obložene tablete
Poland (PL)
Vimetsi
Latvia (LV)
Vimetso 50 mg/850 mg apvalkotās tabletes
Lithuania (LT)
Vimetso 50 mg/850 mg plėvele dengtos tabletės
Estonia (EE)
许可日期
2021/06/16
最近更新日期
2025/05/27
药物ATC编码
A10BD08 metformin and vildagliptin
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 PL
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Final PL
Final SPC
|
Final SPC
PubAR
|
PAR
PubAR Summary
|
PAR Summary
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase