Amoksiklav 1000 mg/200 mg prašak za otopinu za injekciju/infuziju
Name | Amoksiklav 1000 mg/200 mg prašak za otopinu za injekciju/infuziju |
---|---|
Marketing Authorisation Number | HR-H-164490006 |
Active Substance | amoksicilinnatrij kalijev klavulanat |
Composition | jedna bočica sadrži 1000 mg amoksicilina (u obliku natrijeve soli) i 200 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-530-09/17-02/349 |
Registration Number | 381-12-01/70-18-04 |
Prescription | Medicinal product subject to medical prescription |
Type of prescription | ograničeni recept |
Distribution | Supply through pharmacies (community) |
Advertising to general public | not allowed |
ATC Code | J01CR02 |
SmPC | download |
PL | download |