Veterinary Medicines

AviPro ND C131 Lyophilisate for suspension

Authorised
  • Newcastle disease virus, strain Clone 13-1, Live
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Product identification

Medicine name:
AviPro ND C131 Lyophilisate for suspension
Avipro ND C131
Active substance:
  • Newcastle disease virus, strain Clone 13-1, Live
Target species:
  • Turkey
  • Chicken
Route of administration:
  • In drinking water use
  • Topical
  • Ocular use

Product details

Active substance and strength:
  • Newcastle disease virus, strain Clone 13-1, Live
    15848900.00
    50% Embryo Infective Dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate for suspension
Withdrawal period by route of administration:
  • In drinking water use
    • Turkey
      • Meat and offal
        0
        day
      • Egg
        0
        day
    • Chicken
      • Meat and offal
        0
        day
      • Egg
        0
        day
  • Topical
    • Chicken
      • Meat and offal
        0
        day
      • Egg
        0
        day
  • Ocular use
    • Chicken
      • Meat and offal
        0
        day
      • Egg
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Portugal
Package description:
  • (ID8): 1 Box with 10 Bottle (Glass) with 5000 Dose (50000 Dose)
  • (ID7): 1 Box with 1 Bottle (Glass) with 5000 Dose (5000 Dose)
  • (ID11): 1 Box with 1 Bottle (Glass) with 2000 Dose (2000 Dose)
  • (ID12): 1 Box with 10 Bottle (Glass) with 2000 Dose (20000 Dose)

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:
  • Elanco GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Lohmann Animal Health GmbH
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • 780/07RIVPT
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0239/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Cyprus
  • Czechia
  • Estonia
  • France
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
Download

Combined File of all Documents

English (PDF)
Published on: 29/01/2024
Download
Portuguese (PDF)
Published on: 19/01/2023
Download
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