Veterinary Medicine Information website

Enterisol Ileitis lyophilisate and diluent for oral suspension for pigs

Authorised
  • Lawsonia intracellularis, strain MS B3903, Live
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Product identification

Medicine name:
Enterisol Ileitis lyophilisate and diluent for oral suspension for pigs
Active substance:
  • Lawsonia intracellularis, strain MS B3903, Live
Target species:
  • Pig
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Lawsonia intracellularis, strain MS B3903, Live
    79433.00
    50% tissue culture infectious dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and solvent for oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Pig
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AE04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Package description:
  • (ID2): 1 Box with (1 Bottle (Glass) with 10 Dose and 1 Bottle (High Density PolyEthylene) with 20 millilitre(s)) (10.0 Dose, 20.0 millilitre(s))
  • (ID4): 1 Box with (1 Bottle (Glass) with 50 Dose and 1 Bottle (High Density PolyEthylene) with 100 millilitre(s)) (50.0 Dose, 100.0 millilitre(s))
  • (ID6): 1 Box with (1 Bottle (Glass) with 100 Dose and 1 Bottle (High Density PolyEthylene) with 200 millilitre(s)) (100.0 Dose, 200.0 millilitre(s))
  • (ID8): 1 Box with 12 Box with (1 Bottle (Glass) with 100 Dose and 1 Bottle (High Density PolyEthylene) with 200 millilitre(s)) (1200.0 Dose, 2400.0 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:
  • Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Vetmedica GmbH
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/042/MR/08-S
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0236/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Slovak (PDF)
Published on: 30/09/2024
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Summary of Product Characteristics

English (PDF)
Published on: 14/02/2022
Updated on: 13/03/2026
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