Veterinary Medicines Information website

Trichoben, lyophilisate and solvent for suspension for injection for cattle

Authorised
  • Trichophyton verrucosum, strain Bodin 1902, Live
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Product identification

Medicine name:
Trichoben, lyophilisate and solvent for suspension for injection for cattle
Active substance:
  • Trichophyton verrucosum, strain Bodin 1902, Live
Target species:
  • Cattle
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Trichophyton verrucosum, strain Bodin 1902, Live
    6.00
    unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Concentrate and solvent for suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        14
        day
      • Meat and offal
        14
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02A
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • Diluent A is supplied in vials of hydrolytic quality II sealed with rubber stopper and aluminium cap presentation 80 ml in 100-ml vial
  • Diluent A is supplied in vials of hydrolytic quality II sealed with rubber stopper and aluminium cap presentation 10 ml in 10-ml vial
  • Diluent A is supplied in vials of hydrolytic quality I sealed with rubber stopper and aluminium cap resentation 40 ml in 50-ml vial
  • Diluent A is supplied in vials of hydrolytic quality I sealed with rubber stopper and aluminium cap presentation 80 ml in 100-ml vial
  • Diluent A is supplied in vials of hydrolytic quality I sealed with rubber stopper and aluminium cap presentation 10 ml in 10-ml vial
  • Vaccine is supplied in the freeze-dried state in 10-ml vials, hydrolytic quality I, sealed with rubber stopper and aluminium cap
  • Vaccine is supplied in the freeze-dried state in 10-ml vials, hydrolytic quality I, sealed with rubber stopper and aluminium Flip off
  • Diluent A is supplied in vials of hydrolytic quality II sealed with rubber stopper and aluminium cap resentation 40 ml in 50-ml vial
  • Carton box containing 1 x 40 ml (after reconstitution) and corresponding amounts of Diluent A
  • Carton box containing 5 x 10 ml (after reconstitution) and corresponding amounts of Diluent A
  • Carton box containing 1 x 80 ml (after reconstitution) and corresponding amounts of Diluent A

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Kernfarm B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 121040
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0233/001
Concerned member states:
  • Belgium

Documents

Combined File of all Documents

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Dutch (PDF)
Published on: 25/01/2022
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