Veterinary Medicines Information website

PORCILIS M HYO, SUSPENSION FOR INJECTION

Not authorised
  • Mycoplasma hyopneumoniae, strain 11, Inactivated
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Product identification

Medicine name:
PORCILIS M HYO, SUSPENSION FOR INJECTION
Active substance:
  • Mycoplasma hyopneumoniae, strain 11, Inactivated
Target species:
  • Pig (for fattening)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Mycoplasma hyopneumoniae, strain 11, Inactivated
    7.00
    log2 antibody unit(s)
    /
    1.00
    unit(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig (for fattening)
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB13
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Austria
Package description:
  • Cardboard boxes with 1 PET vial of 20 ml (10 doses)
  • Cardboard boxes with 5 PET vials of 20 ml (10 doses)
  • Cardboard boxes with 10 PET vials of 20 ml (10 doses)
  • Cardboard boxes with 1 PET vial of 50 ml (25 doses)
  • Cardboard boxes with 5 PET vials of 50 ml (25 doses)
  • Cardboard boxes with 10 PET vials of 50 ml (25 doses)
  • Cardboard boxes with 1 PET vial of 100 ml (50 doses)
  • Cardboard boxes with 5 PET vials of 100 ml (50 doses)
  • Cardboard boxes with 10 PET vials of 100 ml (50 doses)
  • Cardboard boxes with 1 PET vial of 200 ml (100 doses)
  • Cardboard boxes with 5 PET vials of 200 ml (100 doses)
  • Cardboard boxes with 10 PET vials of 200 ml (100 doses)
  • Cardboard boxes with 1 PET vial of 250 ml (125 doses)
  • Cardboard boxes with 5 PET vials of 250 ml (125 doses)
  • Cardboard boxes with 10 PET vials of 250 ml (125 doses)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Intervet Ges.m.b.H.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 8-20284
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0158/001

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 21/06/2013
Updated on: 26/11/2024
Download

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 21/06/2013
Updated on: 26/11/2024
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 21/06/2013
Updated on: 26/11/2024
Download