Cronyxin Injection 50 mg/ml Solution for Injection
Cronyxin Injection 50 mg/ml Solution for Injection
Authorised
- Flunixin meglumine
Product identification
Medicine name:
Cronyxin Injection 50 mg/ml Solution for Injection
Active substance:
- Flunixin meglumine
Target species:
-
Cattle
-
Horse
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Flunixin meglumine82.96/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal31day
-
Milk36hour
-
-
-
Intravenous use
-
Cattle
-
Meat and offal4day
-
Milk24hour
-
-
Horse
-
Meat and offal5day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AG90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- 100 ml clear, Type I glass, multidose vial, with bromobutyl rubber bung and aluminum overseal.
- 50 ml clear, Type I glass, multidose vial, with bromobutyl rubber bung and aluminum overseal.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent (abridged application) - Council Directive 81/851/EEC
Marketing authorisation holder:
- Bimeda Animal Health Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Labiana Life Sciences S.A.
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA22033/040/001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
