Veterinary Medicines

AquaVac 6 emulsion for injection for Atlantic salmon

Authorised
  • Moritella viscosa, Inactivated
  • Vibrio anguillarum, serotype O2A, Inactivated
  • Vibrio anguillarum, serotype O1, Inactivated
  • Aliivibrio salmonicida, Inactivated
  • Aeromonas salmonicida, Inactivated
  • Infectious pancreatic necrosis virus, Inactivated
Download as PDF

Product identification

Medicine name:
AquaVac 6 emulsion for injection for Atlantic salmon
AquaVac 6 emulsion for injection for Atlantic salmon
Active substance:
  • Moritella viscosa, Inactivated
  • Vibrio anguillarum, serotype O2A, Inactivated
  • Vibrio anguillarum, serotype O1, Inactivated
  • Aliivibrio salmonicida, Inactivated
  • Aeromonas salmonicida, Inactivated
  • Infectious pancreatic necrosis virus, Inactivated
Target species:
  • Atlantic salmon
Route of administration:
  • Intraperitoneal use

Product details

Active substance and strength:
  • Moritella viscosa, Inactivated
    6.50
    log2 enzyme-linked immunosorbent assay unit(s)
    /
    0.10
    millilitre(s)
  • Vibrio anguillarum, serotype O2A, Inactivated
    75.00
    Relative Percentage Survival
    /
    0.10
    millilitre(s)
  • Vibrio anguillarum, serotype O1, Inactivated
    75.00
    Relative Percentage Survival
    /
    0.10
    millilitre(s)
  • Aliivibrio salmonicida, Inactivated
    90.00
    Relative Percentage Survival
    /
    0.10
    millilitre(s)
  • Aeromonas salmonicida, Inactivated
    10.70
    log2 enzyme-linked immunosorbent assay unit(s)
    /
    0.10
    millilitre(s)
  • Infectious pancreatic necrosis virus, Inactivated
    1.50
    enzyme-linked immunosorbent assay unit
    /
    0.10
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intraperitoneal use
    • Atlantic salmon
      • All relevant tissues
        0
        degree day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI10AL02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • Bottles of polyethylene terephthalate (PET) closed with a rubber stopper and aluminium cap.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • INTERVET INTERNATIONAL B.V.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10996/288/001
Date of authorisation status change:
Reference member state:
  • Norway
Procedure number:
  • NO/V/0019/001
Concerned member states:
  • Ireland
  • United Kingdom (Northern Ireland)
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."