Flunixin 50 mg/ml Solution for Injection for Cattle, Horses and Pigs
Flunixin 50 mg/ml Solution for Injection for Cattle, Horses and Pigs
Authorised
- Flunixin meglumine
Product identification
Medicine name:
Flunixin 50 mg/ml Solution for Injection for Cattle, Horses and Pigs
Active substance:
- Flunixin meglumine
Target species:
-
Cattle
-
Horse
-
Pig
Route of administration:
-
Intravenous use
-
Intramuscular use
Product details
Active substance and strength:
-
Flunixin meglumine82.90/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Milk36hour
-
Meat and offal7day
-
-
Horse
-
Milkno withdrawal periodDo not use in mares producing milk for human consumption.
-
Meat and offal7day
-
-
-
Intramuscular use
-
Pig
-
Meat and offal22day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AG90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Available in:
-
Portugal
Package description:
- (ID1) 50 millilitre(s): unspecified outer container with 1 Vial (Glass) with 50 millilitre(s)
- (ID2) 100 millilitre(s): unspecified outer container with 1 Vial (Glass) with 100 millilitre(s)
- (ID3) 250 millilitre(s): unspecified outer container with 1 Vial (Glass) with 250 millilitre(s)
- (ID4) 250 millilitre(s): unspecified outer container with 5 Vial (Glass) each with 50 millilitre(s)
- (ID5) 500 millilitre(s): unspecified outer container with 10 Vial (Glass) each with 50 millilitre(s)
- (ID6) 600 millilitre(s): unspecified outer container with 12 Vial (Glass) each with 50 millilitre(s)
- (ID7) 500 millilitre(s): unspecified outer container with 5 Vial (Glass) each with 100 millilitre(s)
- (ID8) 1000 millilitre(s): unspecified outer container with 10 Vial (Glass) each with 100 millilitre(s)
- (ID9) 1200 millilitre(s): unspecified outer container with 12 Vial (Glass) each with 100 millilitre(s)
- (ID10) 1250 millilitre(s): unspecified outer container with 5 Vial (Glass) each with 250 millilitre(s)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories (Ireland) Limited
- Norbrook Laboratories Limited
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 133/01/08RFVPT
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0325/001
Concerned member states:
-
Iceland
-
Netherlands
-
Portugal
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
