Finadyne 50 mg/ml raztopina za injiciranje
Finadyne 50 mg/ml raztopina za injiciranje
Not authorised
- Flunixin
Product identification
Medicine name:
Finadyne 50 mg/ml raztopina za injiciranje
Active substance:
- Flunixin
Target species:
-
Cattle
-
Horse
-
Pig
Route of administration:
-
Intravenous use
-
Intramuscular use
Product details
Active substance and strength:
-
Flunixin50.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Meat4daymeso: 4 dni
-
Milk24hourmleko: 24 ur
-
-
Horse
-
Meat and offal, milk1day1 dan
-
-
-
Intramuscular use
-
Pig
-
Meat and offal18day18 dni
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AG90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Slovenia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Trirx Segre
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0134/001
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.
Slovenian (PDF)
Published on: 14/11/2021
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 14/11/2021
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 14/11/2021
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