Veterinary Medicine Information website

PARVORUVAX

Authorised
  • Erysipelothrix rhusiopathiae, serotype 2, Inactivated
  • Porcine parvovirus, strain K22, Inactivated
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Product identification

Medicine name:
PARVORUVAX
Active substance:
  • Erysipelothrix rhusiopathiae, serotype 2, Inactivated
  • Porcine parvovirus, strain K22, Inactivated
Target species:
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Erysipelothrix rhusiopathiae, serotype 2, Inactivated
    1.00
    enzyme-linked immunosorbent assay unit
    /
    1.00
    Container
  • Porcine parvovirus, strain K22, Inactivated
    2.00
    haemagglutinating units
    /
    1.00
    Container
Pharmaceutical form:
  • Suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AL01
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • Nature of primary packaging elements:Type I glass bottleLow density polyethylene (LDPE) bottleButyl elastomer closure. Aluminium or aluminium-plastic cap.Packaging intended for sale:100 ml (50-dose) bottle, box of 1 bottle.
  • Nature of primary packaging elements:Type I glass bottleLow density polyethylene (LDPE) bottleButyl elastomer closure. Aluminium or aluminium-plastic cap.Packaging intended for sale:50 ml (25-dose) bottle, box of 1 bottle.
  • Nature of primary packaging elements:Type I glass bottleLow density polyethylene (LDPE) bottleButyl elastomer closure. Aluminium or aluminium-plastic cap.Packaging intended for sale:10 ml (5-dose) bottle, box of 1 bottle.

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:
  • Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva-Phylaxia Zrt.
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10815/052/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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