Veterinary Medicines

Susvac P+Ery Każda dawka szczepionki (2 ml) zawiera: Inaktywowany parwowirus świń, szczep FCV117: nie mniej niż 1:100 HI* Inaktywowane bakterie Erysipelotrix rhusiopathiae, serotyp 2: 50 I.U. *HI – jednostki hamowania hemaglutynacji (badania odpowiedzi serologicznej u kawii domowej) Emulsja do wstrzykiwań

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

Medicine name:
Susvac P+Ery Każda dawka szczepionki (2 ml) zawiera: Inaktywowany parwowirus świń, szczep FCV117: nie mniej niż 1:100 HI* Inaktywowane bakterie Erysipelotrix rhusiopathiae, serotyp 2: 50 I.U. *HI – jednostki hamowania hemaglutynacji (badania odpowiedzi serologicznej u kawii domowej) Emulsja do wstrzykiwań
Active substance:
  • Porcine parvovirus, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, Inactivated
Target species:
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Porcine parvovirus, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, Inactivated
    50.00
    international unit(s)
    /
    2.00
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection/infusion
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AL01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Package description:

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:
  • Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Fatro S.p.A.
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 3303
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Polish (PDF)
Published on: 23/02/2026
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Package Leaflet

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Polish (PDF)
Published on: 23/02/2026
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Labelling

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Polish (PDF)
Published on: 23/02/2026
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