Poulvac IB Primer Oral solution or spray solution after reconstitution of the freeze-dried vaccine in water
Poulvac IB Primer Oral solution or spray solution after reconstitution of the freeze-dried vaccine in water
Authorised
- Infectious bronchitis virus, strain D274, Live
- Infectious bronchitis virus, type Massachusetts, strain H120, Live
Product identification
Medicine name:
Poulvac IB Primer Oral solution or spray solution after reconstitution of the freeze-dried vaccine in water
Active substance:
- Infectious bronchitis virus, strain D274, Live
- Infectious bronchitis virus, type Massachusetts, strain H120, Live
Target species:
-
Chicken
Route of administration:
-
Nebulisation use
-
In drinking water use
-
Oculonasal use
Product details
Active substance and strength:
-
Infectious bronchitis virus, strain D274, Live1000.00/50% Embryo Infective Dose1.00Dose
-
Infectious bronchitis virus, type Massachusetts, strain H120, Live1000.00/50% Embryo Infective Dose1.00Dose
Pharmaceutical form:
-
Lyophilisate for oculonasal suspension/use in drinking water
Withdrawal period by route of administration:
-
Nebulisation use
-
Chicken
-
Meat and offal0day
-
Egg0day
-
-
-
In drinking water use
-
Chicken
-
Egg0day
-
Meat and offal0day
-
-
-
Oculonasal use
-
Chicken
-
Meat and offal0day
-
Egg0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Available in:
-
Portugal
Package description:
- (ID4) 10000 Dose: Box (board) with 10 Bottle each with 1000 Dose, closed with (Aluminium) and (chlorobutylrubber`)
- (ID6) 50000 Dose: Box (board) with 10 Bottle each with 5000 Dose, closed with (Aluminium) and (chlorobutylrubber`)
- (ID5) 25000 Dose: Box (board) with 10 Bottle each with 2500 Dose, closed with (Aluminium) and (chlorobutylrubber`)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Portugal Lda.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Manufacturing & Research Spain S.L.
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 275/89 DGV
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0259/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Estonia
-
Greece
-
Hungary
-
Latvia
-
Lithuania
-
Netherlands
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Sweden
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: 14/11/2025