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Bovilis Huskvac

Intervet Ireland LimitedVPA10996/081/001

Main Information

Trade NameBovilis Huskvac
Active SubstancesInactivated cells and equivalent toxoid of irradiated 3rd stage of dictyocaulus vivipatrous
Dosage FormOral suspension
Licence HolderIntervet Ireland Limited
Licence NumberVPA10996/081/001

Group Information

ATC CodeQI02AN01 dictyocaulus
Therapeutic ClassImmunological - Live Vaccine


License statusAuthorised
Licence Issued22/12/2003
Legal StatusPOM (E): Prescription Only Exempt as defined in relevant national legislation


Summary of Product Characteristics *PDF Version
Package LeafletNo document available
Public Assessment ReportNo document available
VariationsNo document available

* The PDF document, together with the national-specific product information on this page, constitute the authorised SPC
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