Veterinary Medicines

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

Authorised

Pasteurella multocida, protein dO (non-toxic derivative of dermonecrotic toxin), recombinant
Bordetella bronchiseptica, Inactivated

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Product identification

Medicine name:

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

Active substance:

Pasteurella multocida, protein dO (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, protein dO (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
    
    Zero days
- Pig (sow, nullipar)
  - Not applicable
    
    0
    
    day
    
    Zero days

Anatomical therapeutic chemical veterinary (ATCvet) codes:

QI09AB04

Legal status of supply:

Veterinary medicinal product subject to veterinary prescription

Authorisation status:

Valid

Authorised in:

Available in:

Austria
Belgium
Bulgaria
Cyprus
Denmark
France
Germany
Greece
Hungary
Ireland
Italy
Netherlands
Norway
Poland
Portugal
Romania
Slovakia
Slovenia
Spain
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)
Packaging:Vial (polyethylene terephthalate (PET)), Package_size:1 vial, Content:250 ml (125 doses)
Packaging:Vial (polyethylene terephthalate (PET)), Package_size:1 vial, Content:100 ml (50 doses)

Additional information

Entitlement type:

Marketing Authorisation

Legal basis of product authorisation:

Complete application (stand-alone) - Council Directive 81/851/EEC

Marketing authorisation holder:

Intervet International B.V.

Marketing authorisation date:

16/11/2000

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:

23/09/2010

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Combined File of all Documents

English (PDF)

Published on: 22/07/2024

Other languages (24)

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

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

English (PDF)

Published on: 15/03/2023