Veterinary Medicines

AquaVac 6 emulsion for injection for Atlantic salmon

Not authorised
  • Moritella viscosa, Inactivated
  • Vibrio anguillarum, serotype O2a, Inactivated
  • Vibrio anguillarum, serotype O1, Inactivated
  • Aliivibrio salmonicida, Inactivated
  • Aeromonas salmonicida, subsp. 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, subsp. 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, subsp. 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:
  • Surrendered
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