ProteqFlu (--) - Suspension for injection
ProteqFlu (--) - Suspension for injection
Authorised
- Canarypox virus, strain vCP3011, expressing haemagglutinin gene of Influenza A virus subtype H3N8 (A/equine/Richmond/1/2007), Live
- Canarypox virus, strain vCP2242, expressing haemagglutinin gene of Influenza A virus subtype H3N8 (A/equine/Ohio/03), Live
Product identification
Medicine name:
ProteqFlu (--) - Suspension for injection
Active substance:
- Canarypox virus, strain vCP3011, expressing haemagglutinin gene of Influenza A virus subtype H3N8 (A/equine/Richmond/1/2007), Live
- Canarypox virus, strain vCP2242, expressing haemagglutinin gene of Influenza A virus subtype H3N8 (A/equine/Ohio/03), Live
Target species:
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Horse
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Canarypox virus, strain vCP3011, expressing haemagglutinin gene of Influenza A virus subtype H3N8 (A/equine/Richmond/1/2007), LivePresentation_strength:vCP3011 ≥ 10⁵·³ FAID50 Reference:Hse Index:0
-
Canarypox virus, strain vCP2242, expressing haemagglutinin gene of Influenza A virus subtype H3N8 (A/equine/Ohio/03), LivePresentation_strength:vCP2242 ≥ 10⁵·³ FAID50 Reference:Hse Index:1
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
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Horse
-
Not applicable0dayZero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI05AD02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
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Austria
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Belgium
-
Bulgaria
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Croatia
-
Cyprus
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Czechia
-
Denmark
-
Estonia
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Finland
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France
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Germany
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Greece
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Hungary
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Iceland
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Ireland
-
Italy
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Latvia
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Liechtenstein
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Lithuania
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Luxembourg
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Malta
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Netherlands
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Norway
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Poland
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Portugal
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Romania
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Slovakia
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Slovenia
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Spain
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Sweden
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United Kingdom (Northern Ireland)
Available in:
-
Belgium
-
Czechia
-
France
-
Luxembourg
-
Poland
-
Slovakia
-
Spain
Package description:
- Packaging:Vial (glass), Package_size:10 vials, Content:1 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
- Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
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: 21/04/2023
Bulgarian (PDF)
Published on: 21/04/2023
Croatian (PDF)
Published on: 21/04/2023
Czech (PDF)
Published on: 21/04/2023
Danish (PDF)
Published on: 21/04/2023
Dutch (PDF)
Published on: 21/04/2023
Estonian (PDF)
Published on: 21/04/2023
Finnish (PDF)
Published on: 21/04/2023
French (PDF)
Published on: 21/04/2023
German (PDF)
Published on: 21/04/2023
Greek (PDF)
Published on: 21/04/2023
Hungarian (PDF)
Published on: 21/04/2023
Icelandic (PDF)
Published on: 21/04/2023
Italian (PDF)
Published on: 21/04/2023
Latvian (PDF)
Published on: 21/04/2023
Lithuanian (PDF)
Published on: 21/04/2023
Maltese (PDF)
Published on: 21/04/2023
Norwegian (PDF)
Published on: 21/04/2023
Polish (PDF)
Published on: 21/04/2023
Portuguese (PDF)
Published on: 21/04/2023
Romanian (PDF)
Published on: 21/04/2023
Slovak (PDF)
Published on: 21/04/2023
Slovenian (PDF)
Published on: 21/04/2023
Spanish (PDF)
Published on: 21/04/2023
Swedish (PDF)
Published on: 21/04/2023
