VERSICAN PLUS BB ORAL LYOPHILISAT AND SOLVENT FOR ORAL SUSPENSION FOR DOGS
VERSICAN PLUS BB ORAL LYOPHILISAT AND SOLVENT FOR ORAL SUSPENSION FOR DOGS
Authorised
- Water, purified
- Bordetella bronchiseptica, strain 92 B, Live
Product identification
Medicine name:
VERSICAN PLUS BB ORAL LYOPHILISAT AND SOLVENT FOR ORAL SUSPENSION FOR DOGS
Active substance:
- Water, purified
- Bordetella bronchiseptica, strain 92 B, Live
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Water, purified1.00/millilitre(s)1.00Dose
-
Bordetella bronchiseptica, strain 92 B, Live140000000.00/Colony forming unit1.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for oral suspension
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AE01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Plastic box containing 5, vials of 1 dose of lyophilisate and 5, vials of 1ml of solvent
- Plastic box containing 25 vials of 1 dose of lyophilisate and 25 vials of 1ml of solvent
- Plastic box containing 10 vials of 1 dose of lyophilisate and 10 vials of 1ml of solvent
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V544391
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0401/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
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
Summary of Product Characteristics
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Package Leaflet
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Labelling
This document does not exist in this language (English). You can find it in another language below.
eu-puar-frv0401001-mr-rpe777-en.pdf
English (PDF)
Download Published on: 13/03/2026