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Veterinary Medicines

Porcilis AR-T DF (--) - Suspension for injection

Authorised
  • Pasteurella multocida, non-toxic derivative of dermonecrotic toxin, recombinant
  • Bordetella bronchiseptica, Inactivated

Product identification

Medicine name:
Porcilis AR-T DF (--) - Suspension for injection
Active substance:
  • Pasteurella multocida, non-toxic derivative of dermonecrotic toxin, recombinant
  • Bordetella bronchiseptica, Inactivated
Target species:
  • Pig (sow)
  • Pig (sow, nullipar)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Pasteurella multocida, non-toxic derivative of dermonecrotic toxin, recombinant
    Presentation_strength:≥ 6.2 log2 TN. titre Reference:Hse Index:0
  • Bordetella bronchiseptica, Inactivated
    Presentation_strength:≥ 5.5 log2 Aggl.titre Reference:Hse Index:1
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig (sow)
      • Not applicable
        0
        day
    • Pig (sow, nullipar)
      • Not applicable
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB04
Authorisation status:
  • Valid
Authorised in:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)
Package description:
  • Packaging:Vial (polyethylene terephthalate (PET)), Package_size:1 vial, Content:50 ml (25 doses)
  • Packaging:Vial (polyethylene terephthalate (PET)), Package_size:1 vial, Content:20 ml (10 doses)
  • Packaging:Vial (type I glass), Package_size:1 vial, Content:50 ml (25 doses)
  • Packaging:Vial (type I glass), Package_size:1 vial, Content:20 ml (10 doses)

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:
  • European Commission
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Combined File of all Documents

English (PDF)
Published on: 22/07/2024
Download
Bulgarian (PDF)
Published on: 22/07/2024
Croatian (PDF)
Published on: 22/07/2024
Czech (PDF)
Published on: 22/07/2024
Danish (PDF)
Published on: 22/07/2024
Dutch (PDF)
Published on: 22/07/2024
Estonian (PDF)
Published on: 22/07/2024
Finnish (PDF)
Published on: 22/07/2024
French (PDF)
Published on: 22/07/2024
German (PDF)
Published on: 22/07/2024
Greek (PDF)
Published on: 22/07/2024
Hungarian (PDF)
Published on: 22/07/2024
Icelandic (PDF)
Published on: 22/07/2024
Italian (PDF)
Published on: 22/07/2024
Latvian (PDF)
Published on: 22/07/2024
Lithuanian (PDF)
Published on: 22/07/2024
Maltese (PDF)
Published on: 22/07/2024
Norwegian (PDF)
Published on: 22/07/2024
Polish (PDF)
Published on: 22/07/2024
Portuguese (PDF)
Published on: 22/07/2024
Romanian (PDF)
Published on: 22/07/2024
Slovak (PDF)
Published on: 22/07/2024
Slovenian (PDF)
Published on: 22/07/2024
Spanish (PDF)
Published on: 22/07/2024
Swedish (PDF)
Published on: 22/07/2024

ema-puar-porcilis-ar-t-df-v-055-var-x-0009-en.pdf

English (PDF)
Published on: 15/03/2023
Download

ema-puar-porcilis-ar-t-df-v-055-par-en.pdf

English (PDF)
Published on: 15/03/2023
Download
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