ALIVIOS, flunixin meglumina, soluzione iniettabile per bovini, suini ed equini
ALIVIOS, flunixin meglumina, soluzione iniettabile per bovini, suini ed equini
Authorised
- Flunixin meglumine
Product identification
Medicine name:
ALIVIOS, flunixin meglumina, soluzione iniettabile per bovini, suini ed equini
Active substance:
- Flunixin meglumine
Target species:
-
Cattle
-
Pig
-
Horse (food producing)
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Flunixin meglumine82.95milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Milk48hourpari a 4 mungiture
-
Meat and offal7day
-
- Pig
-
Meat and offal18day
-
- Horse (food producing)
-
Meat and offal7dayUso non autorizzato in equidi che producono alimenti per il consumo umano
-
-
Intravenous use
- Cattle
-
Milk48hourpari a 4 mungiture
-
Meat and offal7day
-
- Pig
-
Meat and offal18day
-
- Horse (food producing)
-
Meat and offal7dayUso non autorizzato in equidi che producono alimenti per il consumo umano
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AG90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Available in:
-
Italy
Package description:
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
- Available only in Italian
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:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 25/01/2024
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