Veterinary Medicines

Buprevet 0.3 mg/ml Solution for Injection for Dogs and Cats

Authorised
  • Buprenorphine hydrochloride
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Product identification

Medicine name:
Buprevet 0,3 mg/ml Injektionslösung für Hunde und Katzen
Buprevet 0.3 mg/ml Solution for Injection for Dogs and Cats
Active substance:
  • Buprenorphine hydrochloride
Target species:
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Buprenorphine hydrochloride
    0.32
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN02AE01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • United Kingdom (Northern Ireland)
Package description:
  • Clear glass vials type II, bromobutyl rubber stopper type I, coated, aluminium cap, Package size: 10 x 2 ml
  • Clear glass vials type II, bromobutyl rubber stopper type I, coated, aluminium cap, Package size: 3 x 2 ml
  • Clear glass vials type II, bromobutyl rubber stopper type I, coated, aluminium cap, Package size: 4 x 2 ml
  • Clear glass vials type II, bromobutyl rubber stopper type I, coated, aluminium cap, Package size: 5 x 2 ml
  • Clear glass vials type II, bromobutyl rubber stopper type I, coated, aluminium cap, Package size: 6 x 2 ml

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:
  • Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetviva Richter GmbH
Responsible authority:
  • The Veterinary Medicines Directorate
Authorisation number:
  • Vm 57446/4007
Date of authorisation status change:
Reference member state:
  • Austria
Procedure number:
  • AT/V/0013/002
Concerned member states:
  • United Kingdom (Northern Ireland)