Veterinary Medicines

Nobilis Paramyxo P201 Emulsion for injection

Authorised
  • Pigeon paramyxovirus 1, strain P201, Inactivated
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Product identification

Medicine name:
Nobilis Paramyxo P201 Emulsion for injection
Nobilis Paramyxo P201 Emulsie voor injectie
Nobilis Paramyxo P201 Emulsion injectable
Nobilis Paramyxo P201 Emulsion zur Injektion
Active substance:
  • Pigeon paramyxovirus 1, strain P201, Inactivated
Target species:
  • Pigeon
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Pigeon paramyxovirus 1, strain P201, Inactivated
    6.80
    log2 haemagglutination inhibiting unit(s)
    /
    0.25
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Pigeon
      • Meat and offal
        0
        day
      • Egg
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01EA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • (ID3): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 250 millilitre(s) (250 millilitre(s))
  • (ID2): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 50 millilitre(s) (50 millilitre(s))
  • (ID1): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 20 millilitre(s) (20 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:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V255744
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0219/001
Concerned member states:
  • Belgium
  • Denmark
  • France
  • Greece
  • Italy
  • Lithuania
  • Luxembourg
  • Netherlands
  • Portugal
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
Updated on: 24/03/2023
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Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 27/11/2025
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French (PDF)
Published on: 27/11/2025
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German (PDF)
Published on: 27/11/2025
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