Veterinary Medicines

Equip Artervac Emulsion for Injection for Horses and Ponies

Authorised
  • Equine arteritis virus, strain Bucyrus, Inactivated
  • Equine arteritis virus, strain Bucyrus, Inactivated
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Product identification

Medicine name:
Equip Artervac Emulsion for Injection for Horses and Ponies
Equip Artervac
Active substance:
  • Equine arteritis virus, strain Bucyrus, Inactivated
  • Equine arteritis virus, strain Bucyrus, Inactivated
Target species:
  • Horse
  • Horse (pony)
Route of administration:
  • Intramuscular use
  • Intramuscular use

Product details

Active substance and strength:
  • Equine arteritis virus, strain Bucyrus, Inactivated
    1.80
    relative unit(s)
    /
    1.00
    millilitre(s)
  • Equine arteritis virus, strain Bucyrus, Inactivated
    1.80
    relative unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
  • Intramuscular use
    • Horse (pony)
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI05AA07
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Package description:
  • (ID3) 2 millilitre(s): Box (Cardboard) with 2 Syringe (Glass) each with 1 millilitre(s)
  • (ID2) 10 millilitre(s): Box (Cardboard) with 10 Syringe (Glass) each with 1 millilitre(s)
  • (ID1) 1 millilitre(s): Box (Cardboard) with 1 Syringe (Glass) with 1 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:
  • Zoetis Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Paul-Ehrlich-Institut
Authorisation number:
  • PEI.V.01240.01.1
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0235/001
Concerned member states:
  • France
  • Ireland
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 7/11/2024
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German (PDF)
Published on: 6/11/2025
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