SynVet-50; 50 mg solution for injection for horses
SynVet-50; 50 mg solution for injection for horses
Authorised
- SODIUM HYALURONATE
Product identification
Medicine name:
SynVet-50; 50 mg solution for injection for horses
Active substance:
- SODIUM HYALURONATE
Target species:
-
Horse
Route of administration:
-
Intraarticular use
Product details
Active substance and strength:
-
SODIUM HYALURONATE50.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intraarticular use
-
Horse
-
Meat and offal0day
-
Milk0hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM09AX01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
Package description:
- Single-dose glass syringe barrel with luer tip and rigid tip capType 1 glass syringe, lubricated with dimethicone. Styrene-butadiene rubber cap.Bromobutyl rubber plunger.Available as multipack with six single dose cartons aggregated and overwrapped with plastic foil and label.
- Single-dose glass syringe barrel with luer tip and rigid tip capType 1 glass syringe, lubricated with dimethicone. Styrene-butadiene rubber cap.Bromobutyl rubber plunger.Available as single dose syringe in a sealed translucent plastic blister packed in one carton folding box.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Equi Pharma Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- CROMA-PHARMA GmbH
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 835725
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0580/001
Concerned member states:
-
Austria
-
Belgium
-
Denmark
-
France
-
Germany
-
Netherlands
-
Norway
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
English (PDF)
Download Published on: 14/03/2026
German (PDF)
Published on: 2/09/2025
Updated on: 8/04/2026
Summary of Product Characteristics
English (PDF)
Download Published on: 7/06/2026
German (PDF)
Published on: 28/02/2025
Updated on: 8/04/2026
Labelling
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 2/07/2020
Updated on: 8/04/2026
Combined File of all Documents
English (PDF)
Download Published on: 7/06/2026