Veterinary Medicines

GRIPORK emulsion for injection for pigs

Authorised
  • Influenza A virus, subtype H1N1, strain OLL (swine), Inactivated
  • Influenza A virus, subtype H3N2, strain G (swine), Inactivated
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Product identification

Medicine name:
GRIPORK EMULSION INYECTABLE PARA PORCINO
GRIPORK emulsion for injection for pigs
Active substance:
  • Influenza A virus, subtype H1N1, strain OLL (swine), Inactivated
  • Influenza A virus, subtype H3N2, strain G (swine), Inactivated
Target species:
  • Pig
  • Pig (weaned piglet)
  • Pig (female)
  • Pig (male for reproduction)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Influenza A virus, subtype H1N1, strain OLL (swine), Inactivated
    50.00
    haemagglutination inhibiting unit(s)
    /
    1.00
    Dose
  • Influenza A virus, subtype H3N2, strain G (swine), Inactivated
    50.00
    haemagglutination inhibiting unit(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        0
        day
    • Pig (weaned piglet)
      • Meat and offal
        0
        day
    • Pig (female)
      • Meat and offal
        0
        day
    • Pig (male for reproduction)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AA03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Spain
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratorios Hipra S.A.
Responsible authority:
  • Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 2526 ESP
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0470/001/MR
Concerned member states:
  • France
  • Ireland

Documents

Summary of Product Characteristics

English (PDF)
Published on: 17/11/2025
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Spanish (PDF)
Published on: 17/11/2025
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Package Leaflet

English (PDF)
Published on: 17/11/2025
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Spanish (PDF)
Published on: 17/11/2025
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Labelling

English (PDF)
Published on: 17/11/2025
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Spanish (PDF)
Published on: 17/11/2025
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