GENTIPRAMOX (150+40)MG/ML ΕΝΕΣΙΜΟ ΕΝΑΙΩΡΗΜΑ
GENTIPRAMOX (150+40)MG/ML ΕΝΕΣΙΜΟ ΕΝΑΙΩΡΗΜΑ
Authorised
- Gentamicin sulfate
- Amoxicillin trihydrate
Product identification
Medicine name:
GENTIPRAMOX (150+40)MG/ML ΕΝΕΣΙΜΟ ΕΝΑΙΩΡΗΜΑ
Active substance:
- Gentamicin sulfate
- Amoxicillin trihydrate
Target species:
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Gentamicin sulfate40.00/milligram(s)1.00millilitre(s)
-
Amoxicillin trihydrate150.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal30day
-
Milk2day
-
-
Pig
-
Meat and offal30day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01RA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Hipra S.A.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 65467/20-09-2012/K-0132501
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet