Vetaflumex 50 mg/ml, solução injectável para bovinos, equinos e suínos
Vetaflumex 50 mg/ml, solução injectável para bovinos, equinos e suínos
Authorised
- Flunixin meglumine
- Flunixin meglumine
Product identification
Medicine name:
Vetaflumex 50 mg/ml, solução injectável para bovinos, equinos e suínos
Vetaflumex 50 mg/ml, injekcinis tirpalas galvijams, arkliams ir kiaulėms
Active substance:
- Flunixin meglumine
- Flunixin meglumine
Target species:
-
Pig
-
Cattle
-
Horse
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Flunixin meglumine83.00/milligram(s)1.00millilitre(s)
-
Flunixin meglumine83.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal20day
-
-
-
Intravenous use
-
Cattle
-
Meat and offal4day
-
Milk1day
-
-
Horse
-
Meat and offal1day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AG90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Available in:
-
Lithuania
Package description:
- Polypropylene bottles closed with a rubber stopper oversealed with aluminium caps with a capacity of 50 ml.
- Polypropylene bottles closed with a rubber stopper oversealed with aluminium caps with a capacity of 100 ml.
- Polypropylene bottles closed with a rubber stopper oversealed with aluminium caps with a capacity of 250 ml.
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:
- Przedsiebiorstwo Wielobranzowe Vet-Agro Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Vet-Agro Trading Sp. z o.o.
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/14/2263/001-003
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/0116/001
Concerned member states:
-
Bulgaria
-
Greece
-
Hungary
-
Lithuania
-
Romania
-
Slovakia
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet