Veterinary Medicines

Bovilis Rotavec Corona Emulsion for Injection for Cattle

Not authorised
  • Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), strain CN7985, Inactivated
  • Bovine coronavirus, strain Mebus, Inactivated
  • Bovine rotavirus A, type G6P5, strain UK-Compton, Inactivated
Download as PDF

Product identification

Medicine name:
Bovilis Rotavec Corona Emulsion for Injection for Cattle
Bovilis Rotavec Corona Emulsion for Injection for Cattle
Active substance:
  • Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), strain CN7985, Inactivated
  • Bovine coronavirus, strain Mebus, Inactivated
  • Bovine rotavirus A, type G6P5, strain UK-Compton, Inactivated
Target species:
  • Cattle
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), strain CN7985, Inactivated
    560.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
  • Bovine coronavirus, strain Mebus, Inactivated
    340.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
  • Bovine rotavirus A, type G6P5, strain UK-Compton, Inactivated
    874.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
Pharmaceutical form:
  • Emulsion 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:
  • QI02AL01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Malta
Package description:
  • (ID3) 40 millilitre(s): Box (Cardboard) with 1 Vial (Glass) with 40 millilitre(s)
  • (ID4) 100 millilitre(s): Box (Cardboard) with 1 Vial (Glass) with 100 millilitre(s)
  • (ID2) 10 millilitre(s): Box (Cardboard) with 1 Vial (Glass) with 10 millilitre(s)
  • (ID1) 20 millilitre(s): Box (Cardboard) with 10 Vial (Glass) each with 2 millilitre(s)
  • (ID5) 10 millilitre(s): Box (Cardboard) with 1 Vial (PolyEthylene TerePhthalate) with 10 millilitre(s)
  • (ID6) 40 millilitre(s): Box (Cardboard) with 1 Vial (PolyEthylene TerePhthalate) with 40 millilitre(s)
  • (ID7) 100 millilitre(s): Box (Cardboard) with 1 Vial (PolyEthylene TerePhthalate) with 100 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:
  • European Medicines Agency
Marketing authorisation date:
Manufacturing sites for batch release:
  • Burgwedel Biotech GmbH
  • Intervet International B.V.
Responsible authority:
  • Veterinary And Phytosanitary Regulation Department
Authorisation number:
  • VMA
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0276/001