WELLICOX 50 MG/ML SOLUTION FOR INJECTION FOR CATTLE, HORSES, PIGS
WELLICOX 50 MG/ML SOLUTION FOR INJECTION FOR CATTLE, HORSES, PIGS
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
Wellicox 50 mg/ml Solution injectable
Wellicox 50 mg/ml Injektionslösung
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:
-
Valid
Authorised in:
-
Belgium
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
Marketing authorisation date:
Manufacturing sites for batch release:
- CEVA SANTE ANIMALE - LIBOURNE
- Vetem SPA
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0241/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Czechia
-
Denmark
-
Germany
-
Hungary
-
Italy
-
Netherlands
-
Poland
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Portugal
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Romania
-
Sweden
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United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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Labelling
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