PHARMAVAC PHA emulsion for injection for pigeons
PHARMAVAC PHA emulsion for injection for pigeons
Authorised
- Pigeon paramyxovirus 1, strain 988M, Inactivated
- Pigeon herpesvirus, strain V298/70, Inactivated
- Fowl aviadenovirus 8, strain M2/E, Inactivated
Product identification
Medicine name:
PHARMAVAC PHA emulsion for injection for pigeons
PHARMAVAC PHA injekčná emulzia pre holuby
Active substance:
- Pigeon paramyxovirus 1, strain 988M, Inactivated
- Pigeon herpesvirus, strain V298/70, Inactivated
- Fowl aviadenovirus 8, strain M2/E, Inactivated
Target species:
-
Pigeon
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Pigeon paramyxovirus 1, strain 988M, Inactivated6.90/log2 haemagglutination inhibiting unit(s)0.30millilitre(s)
-
Pigeon herpesvirus, strain V298/70, Inactivated38.10/enzyme-linked immunosorbent assay unit0.30millilitre(s)
-
Fowl aviadenovirus 8, strain M2/E, Inactivated24.70/enzyme-linked immunosorbent assay unit0.30millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Pigeon
-
All relevant tissues0dayZero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01EA
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Package description:
- Paper carton containing one glass vial, type I closed with chlorobutyl rubber stopper sealed with aluminium cap
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:
- Pharmagal Bio spol. s r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Pharmagal Bio spol. s r.o.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/055/DC/18
Date of authorisation status change:
Reference member state:
-
Slovakia
Procedure number:
- SK/V/0108/001
Concerned member states:
-
Belgium
-
Czechia
-
Germany
-
Hungary
-
Netherlands
-
Poland
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: 3/12/2021
Slovak (PDF)
Published on: 10/09/2025