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 | na recept |
Type of prescription | ograničeni recept |
Distribution | u ljekarni |
Advertising to general public | zabranjeno |
ATC Code | J01CR02 |
Medicinal product marketed in the Croatia | Ne |
SmPC | download |
PL | download |