Eliskardia 5 mg filmom obložene tablete
Name | Eliskardia 5 mg filmom obložene tablete |
---|---|
Marketing Authorisation Number | HR-H-869691851 |
Active Substance | prasugrel |
Composition | jedna filmom obložena tableta sadrži 5 mg prasugrela |
Pharmaceutical Form | filmom obložena tableta |
Packaging [MA Number for Packaging] | 14 tableta u blisteru, u kutiji [HR-H-869691851-01] 28 tableta u blisteru, u kutiji [HR-H-869691851-02] 30 tableta u blisteru, u kutiji [HR-H-869691851-03] 56 tableta u blisteru, u kutiji [HR-H-869691851-04] 60 tableta u blisteru, u kutiji [HR-H-869691851-05] 84 tablete u blisteru, u kutiji [HR-H-869691851-06] 90 tableta u blisteru, u kutiji [HR-H-869691851-07] 98 tableta u blisteru, u kutiji [HR-H-869691851-08] |
Manufacturer | Krka d.d., Novo mesto, Slovenija |
Marketing Authorisation Holder | Krka - farma d.o.o., Radnička cesta 48, Zagreb |
Marketing Authorisation Date | 17.09.2018 |
MA Period of Validity | 17.09.2023 |
Classification Number | UP/I-530-09/17-01/62 |
Registration Number | 381-12-01/70-18-04 |
Prescription | na recept |
Type of prescription | ponovljivi recept |
Distribution | u ljekarni |
Advertising to general public | zabranjeno |
ATC Code | B01AC22 |
Medicinal product marketed in the Croatia | Ne |
SmPC | download |
PL | download |
Public Assessment Report | download |
Educational materials for healthcare professionals |
Vodič za zdravstvene radnike, verzija 1 |