欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1550/003
药品名称
Jimandin
活性成分
Sitagliptin 100.0 mg
剂型
Film-coated tablet
上市许可持有人
Medochemie Ltd. Cyprus
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Greece (GR)
JIMANDIN
Latvia (LV)
Jimandin 100 mg apvalkotās tabletes
Lithuania (LT)
JIMANDIN 100 mg plėvele dengtos tabletės
Bulgaria (BG)
Jimandin
Cyprus (CY)
Czechia (CZ)
JIMANDIN
Romania (RO)
JIMANDIN 100 mg comprimate filmate
Slovakia (SK)
JIMANDIN 100 mg filmom obalené tablety
Malta (MT)
Jimandin 100 mg film-coated tablets
Croatia (HR)
Jimandin 100 mg filmom obložene tablete
许可日期
2017/06/21
最近更新日期
2025/04/02
药物ATC编码
A10BH01 sitagliptin
申请类型
TypeLevel1:
Known Active Substance
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 PL
|
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