POULVAC MAREK HVT WET CONCENTRADO Y DISOLVENTE PARA SUSPENSION INYECTABLE PARA POLLOS
POULVAC MAREK HVT WET CONCENTRADO Y DISOLVENTE PARA SUSPENSION INYECTABLE PARA POLLOS
Authorised
- Turkey herpesvirus, strain FC-126 (cell-associated), Live
Product identification
Medicine name:
POULVAC MAREK HVT WET CONCENTRADO Y DISOLVENTE PARA SUSPENSION INYECTABLE PARA POLLOS
Active substance:
- Turkey herpesvirus, strain FC-126 (cell-associated), Live
Target species:
-
Chicken (broiler)
-
Chicken (pullet for egg production, future layer)
-
Future breeder pullet
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Turkey herpesvirus, strain FC-126 (cell-associated), Live3.00/plaque forming unit1.00Dose
Pharmaceutical form:
-
Suspension and solvent for suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Chicken (broiler)
-
Meat and offal0day
-
-
Chicken (pullet for egg production, future layer)
-
Meat and offal0day
-
-
Future breeder pullet
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Chicken (broiler)
-
Meat and offal0day
-
-
Chicken (pullet for egg production, future layer)
-
Meat and offal0day
-
-
Future breeder pullet
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Available in:
-
Spain
Package description:
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
- Available only in Spanish
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Spain S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Manufacturing & Research Spain S.L.
- Zoetis Belgium
Responsible authority:
- Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 2775 ESP
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.
Spanish (PDF)
Published on: 11/07/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 11/07/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 11/07/2025