Nobilis Marek THV Lyofilisaat en oplosmiddel voor oplossing voor injectie
Nobilis Marek THV Lyofilisaat en oplosmiddel voor oplossing voor injectie
Not authorised
- Turkey herpesvirus, strain PB-THV-1, Live
Product identification
Medicine name:
Nobilis Marek THV Lyofilisaat en oplosmiddel voor oplossing voor injectie
Nobilis Marek THV Lyophilisat et solvant pour solution injectable
Nobilis Marek THV Lyophilisat und Lösungsmittel zur Herstellung einer Injektionslösung
Active substance:
- Turkey herpesvirus, strain PB-THV-1, Live
Target species:
-
Chicken (chick)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Turkey herpesvirus, strain PB-THV-1, Live1000.00/plaque forming unit0.20millilitre(s)
Pharmaceutical form:
-
Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Chicken (chick)
-
Meat and offalno withdrawal period0 days
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- Nobilis Marek THV 1 Vial with 1000 doses of Lyophilisate and 1 bag with 400 ml of solvent for solution for injection
- Nobilis Marek THV 1 Vial with 500 doses of Lyophilisate and 1 bag with 200 ml of solvent for solution for injection
- Nobilis Marek THV 1 Vial with 1000 doses of Lyophilisate and 1 bag with 500 ml of solvent for solution for injection
- Nobilis Marek THV 1 Vial with 1000 doses of Lyophilisate and 1 vial with 400 ml of solvent for solution for injection
- Nobilis Marek THV 1 Vial with 500 doses of Lyophilisate and 1 vial with 200 ml of solvent for solution for injection
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
How useful was this page?:
