WELLICOX 50 MG/ML SOLUTION FOR INJECTION FOR CATTLE, HORSES, PIGS
WELLICOX 50 MG/ML SOLUTION FOR INJECTION FOR CATTLE, HORSES, PIGS
Not authorised
- Flunixin meglumine
Product identification
Medicine name:
WELLICOX 50 MG/ML SOLUTION FOR INJECTION FOR CATTLE, HORSES, PIGS
Wellicox 50 mg/ml oplossing voor injectie voor runderen, varkens en paarden
Active substance:
- Flunixin meglumine
Target species:
-
Cattle
-
Pig
-
Horse
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Flunixin meglumine83.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal31day
-
Milk36hour
-
-
Pig
-
Meat and offal24day
-
-
-
Intravenous use
-
Cattle
-
Meat and offal4day
-
Milk24hour
-
-
Horse
-
Meat and offal5day
-
Milkno withdrawal periodNot authorised for use in mares producing milk for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AG90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Netherlands
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:
- CEVA Sante Animale B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
- Vetem S.p.A.
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 111392
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0241/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 24/09/2025