Veterinary Medicines

NOBILIS IB MA5

Authorised
  • Avian infectious bronchitis virus, type Massachusetts, strain Ma5, Live
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Product identification

Medicine name:
NOBILIS IB MA5
Active substance:
  • Avian infectious bronchitis virus, type Massachusetts, strain Ma5, Live
Target species:
  • Chicken (hen)
  • Chicken (chick, for replacement)
  • Chicken (broiler)
Route of administration:
  • Nebulisation use
  • In drinking water use
  • Oculonasal use

Product details

Active substance and strength:
  • Avian infectious bronchitis virus, type Massachusetts, strain Ma5, Live
    3.00
    50% Embryo Infective Dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate for oculonasal suspension/use in drinking water
Withdrawal period by route of administration:
  • Nebulisation use
    • Chicken (hen)
      • Meat and offal
        0
        day
    • Chicken (chick, for replacement)
      • Meat and offal
        0
        day
    • Chicken (broiler)
      • Meat and offal
        0
        day
  • In drinking water use
    • Chicken (hen)
      • Meat and offal
        0
        day
    • Chicken (chick, for replacement)
      • Meat and offal
        0
        day
    • Chicken (broiler)
      • Meat and offal
        0
        day
  • Oculonasal use
    • Chicken (hen)
      • Meat and offal
        0
        day
    • Chicken (chick, for replacement)
      • Meat and offal
        0
        day
    • Chicken (broiler)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD07
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Spain
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Merck Sharp & Dohme Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • INTERVET INTERNATIONAL B.V.
Responsible authority:
  • Spanish Agency For Medicines And Health Products
Authorisation number:
  • 2361 ESP
Date of authorisation status change:

Documents

Labelling

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Spanish (PDF)
Published on: 7/03/2024
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 7/03/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 7/03/2024
Download
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