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Porcilis Ery+Parvo+Lepto suspension for injection for pigs

Authorised
  • Leptospira interrogans, serovar Bratislava, strain As-05-073, Inactivated
  • Leptospira santarosai, serovar Gatuni, strain S1148/02, Inactivated
  • Leptospira interrogans, serovar Pomona, strain Po-01-000, Inactivated
  • Leptospira kirschneri, serovar Dadas, strain GR-01-005, Inactivated
  • Leptospira interrogans, serovar Copenhageni, strain Ic-02-001, Inactivated
  • Leptospira interrogans, serovar Portlandvere, strain Ca-12-000, Inactivated
  • Porcine parvovirus, strain 014, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
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Product identification

Medicine name:
Porcilis Ery+Parvo+Lepto suspension for injection for pigs
Active substance:
  • Leptospira interrogans, serovar Bratislava, strain As-05-073, Inactivated
  • Leptospira santarosai, serovar Gatuni, strain S1148/02, Inactivated
  • Leptospira interrogans, serovar Pomona, strain Po-01-000, Inactivated
  • Leptospira kirschneri, serovar Dadas, strain GR-01-005, Inactivated
  • Leptospira interrogans, serovar Copenhageni, strain Ic-02-001, Inactivated
  • Leptospira interrogans, serovar Portlandvere, strain Ca-12-000, Inactivated
  • Porcine parvovirus, strain 014, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
Target species:
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Leptospira interrogans, serovar Bratislava, strain As-05-073, Inactivated
    1310.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
  • Leptospira santarosai, serovar Gatuni, strain S1148/02, Inactivated
    276.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
  • Leptospira interrogans, serovar Pomona, strain Po-01-000, Inactivated
    166.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
  • Leptospira kirschneri, serovar Dadas, strain GR-01-005, Inactivated
    648.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
  • Leptospira interrogans, serovar Copenhageni, strain Ic-02-001, Inactivated
    210.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
  • Leptospira interrogans, serovar Portlandvere, strain Ca-12-000, Inactivated
    2816.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
  • Porcine parvovirus, strain 014, Inactivated
    130.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
  • Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
    1.00
    Protective Dose
    /
    2.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AL07
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovenia
Available in:
  • Slovenia
Package description:
  • (ID6) 250 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 250 millilitre(s)
  • (ID5) 100 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 100 millilitre(s)
  • (ID4) 500 millilitre(s): Box (Cardboard) with 10 Bottle (PolyEthylene TerePhthalate) each with 50 millilitre(s)
  • (ID3) 50 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 50 millilitre(s)
  • (ID2) 200 millilitre(s): Box (Cardboard) with 10 Bottle (PolyEthylene TerePhthalate) each with 20 millilitre(s)
  • (ID1) 20 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 20 millilitre(s)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • DC/V/0554/001
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0268/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • France
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

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Slovenian (PDF)
Published on: 27/11/2024
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Package Leaflet

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Slovenian (PDF)
Published on: 27/11/2024
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 27/11/2024
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