MEFLOSYL injekčný roztok
MEFLOSYL injekčný roztok
Authorised
- Flunixin meglumine
Product identification
Medicine name:
MEFLOSYL injekčný roztok
Active substance:
- Flunixin meglumine
Target species:
-
Horse (non food-producing)
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
Flunixin meglumine83.30/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Horse (non food-producing)
-
All relevant tissuesno withdrawal periodDo not use in horses whose meat is intended 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:
-
Slovakia
Available in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Zoetis Ceska Republika s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Manufacturing & Research Spain S.L.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/047/99-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 10/04/2026