Veterinary Medicine Information website

NOBILIS RISMAVAC + CA 126 SUSPENSION A DILUER ET SOLVANT POUR SUSPENSION INJECTABLE POUR POULES

Authorised
  • Marek's disease virus, serotype 1, strain CVI-988 (Rispens, cell-associated), Live
  • Turkey herpesvirus, strain FC-126 (cell-associated), Live
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Product identification

Medicine name:
NOBILIS RISMAVAC + CA 126 SUSPENSION A DILUER ET SOLVANT POUR SUSPENSION INJECTABLE POUR POULES
Active substance:
  • Marek's disease virus, serotype 1, strain CVI-988 (Rispens, cell-associated), Live
  • Turkey herpesvirus, strain FC-126 (cell-associated), Live
Target species:
  • Chicken (one day-old chick)
  • Chicken (embryonated eggs)
Route of administration:
  • Intramuscular use
  • Subcutaneous use
  • In ovo

Product details

Active substance and strength:
  • Marek's disease virus, serotype 1, strain CVI-988 (Rispens, cell-associated), Live
    3.00
    log10 (50% cell culture infectious dose)/dose
    /
    1.00
    Dose
  • Turkey herpesvirus, strain FC-126 (cell-associated), Live
    3.00
    log10 (50% cell culture infectious dose)/dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Chicken (one day-old chick)
      • All relevant tissues
        0
        day
  • Subcutaneous use
    • Chicken (one day-old chick)
      • All relevant tissues
        0
        day
  • In ovo
    • Chicken (embryonated eggs)
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Available in:
  • France
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
Marketing authorisation date:
Manufacturing sites for batch release:
  • Merck Sharp & Dohme Animal Health S.L.
  • Intervet International B.V.
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/9561987 7/2003
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 27/06/2024
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Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 15/10/2025
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