Amoksiklav 500 mg/100 mg prašak za otopinu za injekciju/infuziju
| Name | Amoksiklav 500 mg/100 mg prašak za otopinu za injekciju/infuziju |
|---|---|
| Marketing Authorisation Number | HR-H-860009817 |
| Active Substance | amoksicilinnatrij kalijev klavulanat |
| Composition | jedna bočica sadrži 500 mg amoksicilina (u obliku natrijeve soli) i 100 mg klavulanske kiseline (u obliku kalijeve soli) |
| Pharmaceutical Form | prašak za otopinu za injekciju/infuziju |
| Manufacturer | Sandoz GmbH, Kundl, Austrija |
| Marketing Authorisation Holder | Sandoz d.o.o., Maksimirska 120, Zagreb, Hrvatska |
| Marketing Authorisation Date | 29.06.2018 |
| MA Period of Validity | unlimited |
| Classification Number | UP/I-530-09/17-02/348 |
| Registration Number | 381-12-01/70-18-06 |
| Prescription | Medicinal product subject to medical prescription |
| Type of prescription | Medicinal product subject to restricted medical prescription |
| Distribution | Supply through pharmacies (community) |
| Advertising to general public | not allowed |
| ATC Code | J01CR02 |
| Marketing status | Never marketed |
| SmPC | download |
| PL | download |
