Equilis Prequenza (--) - Suspension for injection
Equilis Prequenza (--) - Suspension for injection
Authorised
- Influenza A virus, subtype H3N8, strain A/equine/Newmarket/2/93, Inactivated
- Influenza A virus, subtype H3N8, strain A/equine/South Africa/4/03, Inactivated
Product identification
Medicine name:
Equilis Prequenza (--) - Suspension for injection
Active substance:
- Influenza A virus, subtype H3N8, strain A/equine/Newmarket/2/93, Inactivated
- Influenza A virus, subtype H3N8, strain A/equine/South Africa/4/03, Inactivated
Target species:
-
Horse
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Influenza A virus, subtype H3N8, strain A/equine/Newmarket/2/93, InactivatedPresentation_strength:50 AU Reference:II.C.2.1.1.a Comments:induction of immunity Index:0
-
Influenza A virus, subtype H3N8, strain A/equine/South Africa/4/03, InactivatedPresentation_strength:50 AU Reference:II.C.2.1.1.b Comments:induction of immunity Index:1
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Horse
-
Not applicable0dayZero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI05AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Liechtenstein
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
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Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
Available in:
-
Austria
-
Netherlands
-
Norway
-
Poland
-
Sweden
Package description:
- Packaging:Vial (glass), Package_size:10 vials, Content:1 dose
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Annex of Council Regulation (EEC) No 2309/93
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- European Commission
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
English (PDF)
Download Published on: 7/03/2024
Bulgarian (PDF)
Published on: 7/03/2024
Croatian (PDF)
Published on: 7/03/2024
Czech (PDF)
Published on: 7/03/2024
Danish (PDF)
Published on: 7/03/2024
Dutch (PDF)
Published on: 7/03/2024
Estonian (PDF)
Published on: 7/03/2024
Finnish (PDF)
Published on: 7/03/2024
French (PDF)
Published on: 7/03/2024
German (PDF)
Published on: 7/03/2024
Greek (PDF)
Published on: 7/03/2024
Hungarian (PDF)
Published on: 7/03/2024
Icelandic (PDF)
Published on: 7/03/2024
Italian (PDF)
Published on: 7/03/2024
Latvian (PDF)
Published on: 7/03/2024
Lithuanian (PDF)
Published on: 7/03/2024
Maltese (PDF)
Published on: 7/03/2024
Norwegian (PDF)
Published on: 7/03/2024
Polish (PDF)
Published on: 7/03/2024
Portuguese (PDF)
Published on: 7/03/2024
Romanian (PDF)
Published on: 7/03/2024
Slovak (PDF)
Published on: 7/03/2024
Slovenian (PDF)
Published on: 7/03/2024
Spanish (PDF)
Published on: 7/03/2024
Swedish (PDF)
Published on: 7/03/2024
