| Name |
Amoksicilin Belupo 500 mg tablete za oralnu suspenziju |
| Marketing Authorisation Number |
HR-H-380903537 |
| Active Substance |
amoksicilin trihidrat |
| Composition |
jedna tableta za oralnu suspenziju sadrži 500 mg amoksicilina u obliku amoksicilin trihidrata |
| Pharmaceutical Form |
tableta za oralnu suspenziju |
| Manufacturer |
Belupo lijekovi i kozmetika d.d., Koprivnica, Hrvatska |
| Marketing Authorisation Holder |
Belupo lijekovi i kozmetika d.d., Ulica Danica 5, Koprivnica, Hrvatska |
| Marketing Authorisation Date |
17.06.2021 |
| MA Period of Validity |
17.06.2026 |
| Classification Number |
UP/I-530-09/20-01/39 |
| Registration Number |
381-12-01/70-21-04 |
| Prescription |
na recept |
| Type of prescription |
neponovljivi recept
|
| Distribution |
u ljekarni |
| Advertising to general public |
zabranjeno |
| ATC Code |
J01CA04 |
| Medicinal product marketed in the Croatia |
Da |
| SmPC |
download |
| PL |
download |
| Public Assessment Report |
download
|
