SYNULOX 500 mg, kramtomosios tabletės šunims
SYNULOX 500 mg, kramtomosios tabletės šunims
Awtorizzat
- Clavulanic acid
- Amoxicillin
Identifikazzjoni tal-prodott
Isem tal-mediċina:
SYNULOX 500 mg, kramtomosios tabletės šunims
Metodu ta’ amministrazzjoni:
-
Użu orali
Dettalji tal-prodott
Forma farmaċewtika:
-
Pillola li tomgħodha
Withdrawal period by route of administration:
-
Użu orali
-
Dog
-
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QJ01CR02
Status tal-awtorizzazzjoni:
-
Valid
Tagħrif addizzjonali
Marketing authorisation date:
Awtorità responsabbli:
- State Food And Veterinary Service
Numru tal-awtorizzazzjoni:
- B1-989
Parallel trade in reference of:
Parallel trade of:
Source wholesaler:
- Vetmarket SIA
Destination wholesaler:
- Vetmarket UAB
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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