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Veterinary Medicines

PORCILIS LAWSONIA ID LYOPHILISATE AND SOLVENT FOR EMULSION FOR INJECTION FOR PIGS

Authorised
  • Lawsonia intracellularis, strain SPAH-08, Inactivated

Product identification

Medicine name:
PORCILIS LAWSONIA ID LYOPHILISATE AND SOLVENT FOR EMULSION FOR INJECTION FOR PIGS
PORCILIS LAWSONIA ID LYOPHILISAT ET SOLVANT POUR EMULSION INJECTABLE POUR PORCS
Active substance:
  • Lawsonia intracellularis, strain SPAH-08, Inactivated
Target species:
  • Pig
Route of administration:
  • Intradermal use

Product details

Active substance and strength:
  • Lawsonia intracellularis, strain SPAH-08, Inactivated
    5323.00
    unit(s)
    /
    1.00
    unit(s)
Pharmaceutical form:
  • Lyophilisate and solvent for emulsion for injection
Withdrawal period by route of administration:
  • Intradermal use
    • Pig
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB18
Authorisation status:
  • Valid
Authorised in:
  • France
Available in:
  • France
Package description:
  • Cardboard box with 1 x 200 doses of vaccine and cardboard box with 1 x 40 ml solvent
  • Cardboard box with 10 x 200 doses of vaccine and cardboard box with 10 x 40 ml solvent
  • Cardboard box with 10 x 200 doses of vaccine and cardboard box with 10 x 40 ml solvent
  • Cardboard box with 10 x 200 doses of vaccine and cardboard box with 10 x 40 ml solvent
  • Cardboard box with 10 x 200 doses of vaccine and cardboard box with 10 x 40 ml solvent
  • Cardboard box with 10 x 200 doses of vaccine and cardboard box with 10 x 40 ml solvent

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/0617589 2/2020
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0424/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 6/02/2026

Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 6/02/2026

Combined File of all Documents

English (PDF)
Published on: 20/01/2026
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