Icthiovac ERM Concentrate for dip suspension
Icthiovac ERM Concentrate for dip suspension
Authorised
- Yersinia ruckeri, serotype O1, biotype 1, strain 8363, Inactivated
- Yersinia ruckeri, serotype O1, biotype 2, strain 8302, Inactivated
- Yersinia ruckeri, serotype O2, biotype 1, strain 8365, Inactivated
Product identification
Medicine name:
Icthiovac ERM Concentrate for dip suspension
Active substance:
- Yersinia ruckeri, serotype O1, biotype 1, strain 8363, Inactivated
- Yersinia ruckeri, serotype O1, biotype 2, strain 8302, Inactivated
- Yersinia ruckeri, serotype O2, biotype 1, strain 8365, Inactivated
Target species:
-
Atlantic salmon
Route of administration:
-
Dipping
Product details
Active substance and strength:
-
Yersinia ruckeri, serotype O1, biotype 1, strain 8363, InactivatedPresentation_strength:≥10.19 log10 BDC/ml Reference:In House Index:0
-
Yersinia ruckeri, serotype O1, biotype 2, strain 8302, InactivatedPresentation_strength:≥9.91 log10 BDC/ml Reference:In House Index:1
-
Yersinia ruckeri, serotype O2, biotype 1, strain 8365, InactivatedPresentation_strength:≥10.07 log10 BDC/ml Reference:In House Index:2
Pharmaceutical form:
-
Concentrate for dip suspension
Withdrawal period by route of administration:
-
Dipping
-
Atlantic salmon
-
Fish meat0dayZero degree days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI10AB04
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
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Liechtenstein
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
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Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
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Slovenia
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Spain
-
Sweden
-
United Kingdom (Northern Ireland)
Package description:
- Packaging:Bottle (PP), Package_size:1 bottle, Content:1000 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - new active substance (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Laboratorios Hipra, S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Hipra S.A.
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: 7/05/2025
Bulgarian (PDF)
Published on: 7/05/2025
Croatian (PDF)
Published on: 7/05/2025
Czech (PDF)
Published on: 7/05/2025
Danish (PDF)
Published on: 7/05/2025
Dutch (PDF)
Published on: 7/05/2025
Estonian (PDF)
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Finnish (PDF)
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French (PDF)
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German (PDF)
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Greek (PDF)
Published on: 7/05/2025
Hungarian (PDF)
Published on: 7/05/2025
Icelandic (PDF)
Published on: 7/05/2025
Italian (PDF)
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Latvian (PDF)
Published on: 7/05/2025
Lithuanian (PDF)
Published on: 7/05/2025
Maltese (PDF)
Published on: 7/05/2025
Norwegian (PDF)
Published on: 7/05/2025
Polish (PDF)
Published on: 7/05/2025
Portuguese (PDF)
Published on: 7/05/2025
Romanian (PDF)
Published on: 7/05/2025
Slovak (PDF)
Published on: 7/05/2025
Slovenian (PDF)
Published on: 7/05/2025
Spanish (PDF)
Published on: 7/05/2025
Swedish (PDF)
Published on: 7/05/2025
