Veterinary Medicines

Bovilis Huskvac oral suspension for cattle

Authorised
  • Dictyocaulus viviparus, third stage larvae, Live
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Product identification

Medicine name:
Bovilis Huskvac oral suspension for cattle
Active substance:
  • Dictyocaulus viviparus, third stage larvae, Live
Target species:
  • Cattle
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Dictyocaulus viviparus, third stage larvae, Live
    1000.00
    Organisms
    /
    1.00
    Dose
Pharmaceutical form:
  • Oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AN01
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • 25 ml larval suspension in 30 ml glass hydrolytic class type III bottles, closed with a metal screwcap with a PEP facedinlay.Each package presentation consists of 12 x 25 ml (1 dose) bottles.

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:
  • Intervet (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • MSD Animal Health UK Limited
  • Intervet International B.V.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10996/081/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 31/08/2025
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