Innovax-ILT (--) concentrate and solvent for suspension for injection
Innovax-ILT (--) concentrate and solvent for suspension for injection
Authorised
- Turkey herpesvirus, strain HVT/ILT-138 (cell-associated), expressing gD and gI glycoproteins genes of Infectious laryngotracheitis virus, Live
Product identification
Medicine name:
Innovax-ILT (--) concentrate and solvent for suspension for injection
Active substance:
- Turkey herpesvirus, strain HVT/ILT-138 (cell-associated), expressing gD and gI glycoproteins genes of Infectious laryngotracheitis virus, Live
Target species:
-
Chicken
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Turkey herpesvirus, strain HVT/ILT-138 (cell-associated), expressing gD and gI glycoproteins genes of Infectious laryngotracheitis virus, LivePresentation_strength:10³·¹ – 10⁴·¹ PFU Reference:In house Comments:per dose Index:0
Pharmaceutical form:
-
Concentrate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Chicken
-
Not applicable0dayZero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Liechtenstein
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
Available in:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
France
-
Germany
-
Greece
-
Hungary
-
Netherlands
-
Poland
-
Spain
-
United Kingdom (Northern Ireland)
Package description:
- Packaging:Concentrate: ampoule (glass), Package_size:Concentrate: 1 ampoule, Content:Concentrate: 4000 doses
- Packaging:Concentrate: ampoule (glass), Package_size:Concentrate: 1 ampoule, Content:Concentrate: 2000 doses
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - New active substance (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:
- European Commission
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
Combined File of all Documents
English (PDF)
Download Published on: 26/05/2023
Bulgarian (PDF)
Published on: 26/05/2023
Croatian (PDF)
Published on: 26/05/2023
Czech (PDF)
Published on: 26/05/2023
Danish (PDF)
Published on: 26/05/2023
Dutch (PDF)
Published on: 26/05/2023
Estonian (PDF)
Published on: 26/05/2023
Finnish (PDF)
Published on: 26/05/2023
French (PDF)
Published on: 26/05/2023
German (PDF)
Published on: 26/05/2023
Greek (PDF)
Published on: 26/05/2023
Hungarian (PDF)
Published on: 26/05/2023
Icelandic (PDF)
Published on: 26/05/2023
Italian (PDF)
Published on: 26/05/2023
Latvian (PDF)
Published on: 26/05/2023
Lithuanian (PDF)
Published on: 26/05/2023
Maltese (PDF)
Published on: 26/05/2023
Norwegian (PDF)
Published on: 26/05/2023
Polish (PDF)
Published on: 26/05/2023
Portuguese (PDF)
Published on: 26/05/2023
Romanian (PDF)
Published on: 26/05/2023
Slovak (PDF)
Published on: 26/05/2023
Slovenian (PDF)
Published on: 26/05/2023
Spanish (PDF)
Published on: 26/05/2023
Swedish (PDF)
Published on: 26/05/2023
ema-puar-innovax-ilt-v-3869-par-en.pdf
English (PDF)
Download Published on: 14/03/2023
