Colombovac PMV/POX
Colombovac PMV/POX
Authorised
- Newcastle disease virus, strain La Sota, Inactivated
- Pigeonpox virus, strain DD, Live
Product identification
Medicine name:
Colombovac PMV/POX
Active substance:
- Newcastle disease virus, strain La Sota, Inactivated
- Pigeonpox virus, strain DD, Live
Target species:
-
Pigeon
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Newcastle disease virus, strain La Sota, Inactivated19.90antigen unit(s)0.20millilitre(s)
-
Pigeonpox virus, strain DD, Live103.50tissue culture infective dose 500.20millilitre(s)
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Pigeon
-
Meat and offal0dayPombos a partir das 6 semanas de idade
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01EH01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Package description:
- Available only in Portuguese
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:
- 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:
- 597/98 DGV
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
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Portuguese (PDF)
Published on: 15/06/2023
Updated on: 18/06/2023
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