Cronyxin Injection 50 mg/ml Roztwór do wstrzykiwań
Cronyxin Injection 50 mg/ml Roztwór do wstrzykiwań
Authorised
- Flunixin meglumine
Product identification
Medicine name:
Cronyxin Injection 50 mg/ml Roztwór do wstrzykiwań
Active substance:
- Flunixin meglumine
Target species:
-
Horse
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Flunixin meglumine83.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Horse
-
Meat and offal7day
-
-
Cattle
-
Meat and offal7day
-
Milk36hour
-
-
Pig
-
Meat and offal18day
-
-
-
Intravenous use
-
Horse
-
Meat and offal7day
-
-
Cattle
-
Milk36hour
-
Meat and offal7day
-
-
Pig
-
Meat and offal18day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AG90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
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:
- Bimeda Animal Health Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- CROSS VETPHARM GROUP Ltd.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 1454
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 4/02/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 4/02/2022
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