Veterinary Medicines

Bovilis Ringvac <9 and >21 Lyophilisate+solvent for suspension for injection

Authorised
  • Trichophyton verrucosum, strain LTF-130, Live
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Product identification

Medicine name:
Bovilis Ringvac <9 and >21 Lyophilisate+solvent for suspension for injection
Bovilis Ringvac, Lyofilizát a rozpouštědlo pro injekční suspenzi
Active substance:
  • Trichophyton verrucosum, strain LTF-130, Live
Target species:
  • Cattle
  • Cattle (calf)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Trichophyton verrucosum, strain LTF-130, Live
    21000000.00
    cells
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Cattle (calf)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AP01
Legal status of supply:
This information is not available for this product.
Authorisation status:
  • Valid
Authorised in:
  • Czechia
Package description:
  • (ID2) 40 millilitre(s); 40 Dose: Box (Cardboard) with 1 Bottle (Glass) with 40 Dose and 1 Bottle (Glass) with 40 millilitre(s)
  • (ID1) 10 Dose; 10 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 10 Dose and 1 Bottle (Glass) with 10 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 International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • INTERVET INTERNATIONAL B.V.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/142/04-C
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0231/001
Concerned member states:
  • Belgium
  • Bulgaria
  • Cyprus
  • Czechia
  • France
  • Greece
  • Hungary
  • Ireland
  • Luxembourg
  • Poland
  • Portugal
  • Slovakia
  • Slovenia

Documents

Summary of Product Characteristics

English (PDF)
Published on: 14/02/2022
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Czech (PDF)
Published on: 25/10/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 25/10/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 25/10/2022
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