Veterinary Medicines Information website

Bovilis IBR marker inac suspension for injection for cattle

Not authorised
  • Bovine herpesvirus 1, strain GK/D gE gene-deleted, Inactivated
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Product identification

Medicine name:
Bovilis IBR marker inac suspension for injection for cattle
Active substance:
  • Bovine herpesvirus 1, strain GK/D gE gene-deleted, Inactivated
Target species:
  • Cattle
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Bovine herpesvirus 1, strain GK/D gE gene-deleted, Inactivated
    60.00
    enzyme-linked immunosorbent assay unit
    /
    1.00
    Dose
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AA03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Revoked
Authorised in:
  • Portugal
Package description:
  • (ID1) 5 Dose: Box with 1 Container (Glass type I) with 5 Dose
  • (ID2) 5 Dose: Box with 1 Container (polyethylene terephthalate) with 5 Dose
  • (ID3) 50 Dose: Box with 10 Container (Glass type I) each with 5 Dose
  • (ID4) 50 Dose: Box with 10 Container (polyethylene terephthalate) each with 5 Dose
  • (ID6) 10 Dose: Box with 1 Container (Glass type I) with 10 Dose
  • (ID7) 10 Dose: Box with 1 Container (polyethylene terephthalate) with 10 Dose
  • (ID8) 100 Dose: Box with 10 Container (Glass type I) each with 10 Dose
  • (ID9) 100 Dose: Box with 10 Container (polyethylene terephthalate) each with 10 Dose
  • (ID10) 25 Dose: Box with 1 Container (Glass type I) with 25 Dose
  • (ID15) 25 Dose: Box with 1 Container (polyethylene terephthalate) with 25 Dose
  • (ID17) 250 Dose: Box with 10 Container (Glass type I) each with 25 Dose
  • (ID19) 250 Dose: Box with 10 Container (polyethylene terephthalate) each with 25 Dose
  • (ID20) 50 Dose: Box with 1 Container (Glass type I) with 50 Dose
  • (ID21) 50 Dose: Box with 1 Container (polyethylene terephthalate) with 50 Dose
  • (ID22) 500 Dose: Box with 10 Container (Glass type I) each with 50 Dose
  • (ID23) 500 Dose: Box with 10 Container (polyethylene terephthalate) each with 50 Dose
  • (ID24) 100 Dose: Box with 1 Container (Glass type I) with 100 Dose
  • (ID25) 100 Dose: Box with 1 Container (polyethylene terephthalate) with 100 Dose
  • (ID26) 1000 Dose: Box with 10 Container (Glass type I) each with 100 Dose
  • (ID27) 1000 Dose: Box with 10 Container (polyethylene terephthalate) each with 100 Dose

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
  • MSD Animal Health Lda.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • R767/06 DGV
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0237/001

Documents

Combined File of all Documents

English (PDF)
Published on: 10/04/2026
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Portuguese (PDF)
Published on: 17/08/2023
Updated on: 18/08/2023
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