Eradia 125 mg/ml, oral suspension for dogs
Eradia 125 mg/ml, oral suspension for dogs
Authorised
- Metronidazole
Product identification
Medicine name:
Eradia 125 mg/ml, oral suspension for dogs
Eradia 125 mg/ml Suspension zum Eingeben für Hunde
Active substance:
- Metronidazole
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Metronidazole125.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01XD01
- QP51AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
Available in:
-
Austria
Package description:
- 100 ml presentation: white opaque polyethylene terephthalate (PET) bottle equipped with a sampling polypropylene (PP) snap cap with silicon stopper and a 3 ml polypropylene (PP) syringe placed in a carton box
- 30 ml presentation: white opaque polyethylene terephthalate (PET) bottle equipped with a sampling polyethylene (PE) screw cap with PE seal and a 3 ml polypropylene (PP) oral syringe placed in a carton box
- 100 ml presentation: white opaque polyethylene terephthalates (PET) bottle equipped with a sampling Polyethylene (PE) screw cap with PE seal and a 3 ml polypropylene (PP) oral syringe placed in a carton box
- 30 ml presentation: white opaque polyethylene terephthalate (PET) bottle equipped with a sampling polypropylene (PP) snap cap with silicon stopper and a 3 ml polypropylene (PP) syringe placed in a carton box
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Delpharm Huningue S.A.S.
- Virbac
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 838255
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0232/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 16/04/2024
Updated on: 20/01/2026
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 16/04/2024
Updated on: 20/01/2026
Labelling
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 16/04/2024
Updated on: 20/01/2026
Combined File of all Documents
English (PDF)
Download Published on: 9/05/2024
Final PuAR Eradia 125 mg-ml oral suspension for dogs_update 05112023.pdf
English (PDF)
Download Published on: 15/12/2025