Veterinary Medicines

Porcilis ar-t, emulsie voor injectie voor varkens

Authorised
  • Pasteurella multocida, serotype D, dermonecrotic toxin, recombinant
  • Bordetella bronchiseptica, Inactivated
Download as PDF

Product identification

Medicine name:
Porcilis ar-t, emulsie voor injectie voor varkens
Active substance:
  • Pasteurella multocida, serotype D, dermonecrotic toxin, recombinant
  • Bordetella bronchiseptica, Inactivated
Target species:
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Pasteurella multocida, serotype D, dermonecrotic toxin, recombinant
    1.80
    unit(s)
    /
    1.00
    Dose
  • Bordetella bronchiseptica, Inactivated
    1.00
    unit(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB04
Legal status of supply:
  • Medicinal product subject to medical prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Intervet Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • INTERVET INTERNATIONAL B.V.
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 1355
Date of authorisation status change:

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 16/02/2022
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."