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
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, Inactivated6.90log2 haemagglutination inhibiting unit(s)0.30millilitre(s)
-
Pigeon herpesvirus, strain V298/70, Inactivated38.10enzyme-linked immunosorbent assay unit0.30millilitre(s)
-
Fowl aviadenovirus 8, strain M2/E, Inactivated24.70enzyme-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:
-
Germany
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:
- Paul-Ehrlich-Institut
Authorisation number:
- PEI.V.11963.01.1
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
Summary of Product Characteristics
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German (PDF)
Published on: 24/02/2022
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