File downloaded on 2026-05-01
Source URL: https://medicines.health.europa.eu/veterinary/en/600000062120
Authorised

Product identification

Medicine name:
Ovilis Enzovax Lyophilisate and solvent for suspension for injection for sheep
Active substance:
  • Chlamydia abortus, strain 1B (thermosensitive), Live
Target species:
  • Sheep
Route of administration:
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Chlamydia abortus, strain 1B (thermosensitive), Live
    100000.00
    Inclusion forming unit(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Sheep
      • Meat and offal
        7
        day
  • Intramuscular use
    • Sheep
      • Meat and offal
        7
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI04AE01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:
  • (ID3) 10 Dose; 20 millilitre(s): Box (board) with 1 Bottle with 10 Dose, closed with (Gummi) and (Aluminium) and 1 Bottle with 20 millilitre(s)
  • (ID7) 100 Dose; 200 millilitre(s): Box (board) with 1 Bottle with 100 Dose, closed with (Gummi) and (Aluminium) and 1 Bottle with 200 millilitre(s)
  • (ID6) 50 Dose; 100 millilitre(s): Box (board) with 1 Bottle with 50 Dose, closed with (Gummi) and (Aluminium) and 1 Bottle with 100 millilitre(s)
  • (ID4) 20 Dose; 40 millilitre(s): Box (board) with 1 Bottle with 20 Dose, closed with (Gummi) and (Aluminium) and 1 Bottle with 40 millilitre(s)
  • (ID11) 100 Dose; 200 millilitre(s): Box (board) with 1 Bottle with 100 Dose, closed with (Gummi) and (Aluminium) and 1 Bottle (polyethylene terephthalate) with 200 millilitre(s)
  • (ID10) 50 Dose; 100 millilitre(s): Box (board) with 1 Bottle with 50 Dose, closed with (Gummi) and (Aluminium) and 1 Bottle (polyethylene terephthalate) with 100 millilitre(s)
  • (ID8) 10 Dose; 20 millilitre(s): Box (board) with 1 Bottle with 10 Dose, closed with (Gummi) and (Aluminium) and 1 Bottle (polyethylene terephthalate) with 20 millilitre(s)
  • (ID9) 20 Dose; 40 millilitre(s): Box (board) with 1 Bottle with 20 Dose, closed with (Gummi) and (Aluminium) and 1 Bottle (polyethylene terephthalate) with 40 millilitre(s)

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:
  • Intervet Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Paul-Ehrlich-Institut
Authorisation number:
  • 163a/95
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0246/001
Concerned member states:
  • Czechia
  • Portugal
  • Slovakia

Documents

Combined File of all Documents

English (PDF)
Published on: 6/11/2025
Download
German (PDF)
Published on: 14/11/2025
Download