Nobilis E.coli inac Emulsion for Injection for Chickens
Nobilis E.coli inac Emulsion for Injection for Chickens
Authorised
- Escherichia coli, fimbrial adhesin F11
- Escherichia coli, flagellar toxin
Product identification
Medicine name:
NOBILIS E.COLI INAC
Nobilis E.coli inac Emulsion for Injection for Chickens
Active substance:
- Escherichia coli, fimbrial adhesin F11
- Escherichia coli, flagellar toxin
Target species:
-
Chicken
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Escherichia coli, fimbrial adhesin F11100.00microgram(s)0.50millilitre(s)
-
Escherichia coli, flagellar toxin100.00microgram(s)0.50millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Chicken
-
Meat and offal35day
-
Eggno withdrawal periodzero days
-
-
Subcutaneous use
- Chicken
-
Meat and offal35day
-
Eggno withdrawal periodzero days
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AB05
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
United Kingdom (Northern Ireland)
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
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- MSD Animal Health UK Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- The Veterinary Medicines Directorate
Authorisation number:
- Vm 01708/4266
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0017/001
Concerned member states:
-
Austria
-
Belgium
-
France
-
Germany
-
Greece
-
Ireland
-
Italy
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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