Veterinary Medicines

Nobilis ND C2 lyophilisate for oculonasal suspension for chickens

Not authorised
  • Newcastle disease virus, strain C2, Live
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Product identification

Medicine name:
NOBILIS ND C2
Nobilis ND C2 lyophilisate for oculonasal suspension for chickens
Active substance:
  • Newcastle disease virus, strain C2, Live
Target species:
  • Chicken
Route of administration:
  • Oculonasal use
  • Nebulisation use

Product details

Active substance and strength:
  • Newcastle disease virus, strain C2, Live
    5.70
    50% Embryo Infective Dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate for oculonasal suspension
Withdrawal period by route of administration:
  • Oculonasal use
    • Chicken
      • All relevant tissues
        no withdrawal period
  • Nebulisation use
    • Chicken
      • All relevant tissues
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Ireland
Package description:
  • Cardboard box with 1 vial of 500 doses.
  • Cardboard box with 1 vial of 5000 doses.
  • PET plastic boxes with 12 cups of 5000 doses
  • PET plastic boxes with 12 cups of 2500 doses
  • PET plastic boxes with 12 cups of 10000 doses
  • PET plastic boxes with 12 cups of 1000 doses
  • Cardboard box with 1 vial of 25000 doses.
  • Cardboard box with 1 vial of 2500 doses.
  • Cardboard box with 1 vial of 10000 doses.
  • Cardboard box with 1 vial of 1000 doses.
  • Cardboard box with 10 vials of 1000 doses.
  • Cardboard box with 10 vials of 10000 doses.
  • Cardboard box with 10 vials of 2500 doses.
  • Cardboard box with 10 vials of 25000 doses.
  • Cardboard box with 10 vials of 5000 doses.
  • Cardboard box with 10 vials of 500 doses.

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:
  • Intervet (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10996/187/001
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0113/001

Documents

Combined File of all Documents

English (PDF)
Published on: 28/10/2024
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