Veterinary Medicine Information website

NOBILIS E.COLI INAC

Not authorised
  • Escherichia coli, flagellar toxin
  • Escherichia coli, fimbrial adhesin F11

Product identification

Medicine name:
NOBILIS E.COLI INAC
Active substance:
  • Escherichia coli, flagellar toxin
  • Escherichia coli, fimbrial adhesin F11
Target species:
  • Chicken
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Escherichia coli, flagellar toxin
    100.00
    microgram(s)
    /
    1.00
    Dose
  • Escherichia coli, fimbrial adhesin F11
    100.00
    microgram(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Chicken
      • Meat and offal
        35
        day
      • Egg
        0
        day
  • Subcutaneous use
    • Chicken
      • Meat and offal
        35
        day
      • Egg
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AB05
Authorisation status:
  • Surrendered
Authorised in:
  • France
Package description:
  • 250 ml (500 doses) in one glass type II vial closed with a nitryl rubber stopper and sealed with a coded aluminium cap in a cardboard box.
  • 500 ml (1000 doses) in one glass type II vial closed with a nitryl rubber stopper and sealed with a coded aluminium cap in a cardboard box.
  • 500 ml (1000 doses) in one PET vial closed with a nitryl rubber stopper and sealed with a coded aluminium cap in a cardboard box.
  • 250 ml (500 doses) in one PET vial closed with a nitryl rubber stopper and sealed with a coded aluminium cap in a cardboard box.

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Intervet
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/9530446 1/1998
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0017/001

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: 4/04/2022