Escitalopram Grindeks 10 mg filmom obložene tablete
| Name | Escitalopram Grindeks 10 mg filmom obložene tablete |
|---|---|
| Marketing Authorisation Number | HR-H-044449875 |
| Active Substance | escitalopramoksalat |
| Composition | svaka filmom obložena tableta sadrži 10 mg escitaloprama (u obliku escitalopramoksalata) |
| Pharmaceutical Form | Filmom obložena tableta |
| Packaging [MA Number for Packaging] | 14 tableta u blisteru, u kutiji [HR-H-044449875-01] 28 tableta u blisteru, u kutiji [HR-H-044449875-02] 30 tableta u blisteru, u kutiji [HR-H-044449875-03] 56 tableta u blisteru, u kutiji [HR-H-044449875-04] 98 tableta u blisteru, u kutiji [HR-H-044449875-05] 100 tableta u blisteru, u kutiji [HR-H-044449875-06] |
| Manufacturer | HBM Pharma s.r.o., Martin, Slovačka
Grindeks AS, Riga, Latvija |
| Marketing Authorisation Holder | Grindeks AS, Krustpils iela 53, Riga, Latvija |
| Marketing Authorisation Date | 15.06.2023 |
| MA Period of Validity | 15.06.2028 |
| Classification Number | UP/I-530-09/21-01/370 |
| Registration Number | 381-12-01/154-23-07 |
| Prescription | na recept |
| Type of prescription | ponovljivi recept |
| Distribution | u ljekarni |
| Advertising to general public | zabranjeno |
| ATC Code | N06AB10 |
| SmPC | download |
| PL | download |
| Public Assessment Report | download |
