Veterinary Medicines

Bupaq 0,3 mg/ml Injektionslösung für Hunde und Katzen

Authorised
  • Buprenorphine hydrochloride
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Product identification

Medicine name:
Bupaq 0,3 mg/ml Injektionslösung für Hunde und Katzen
Bupaq, 0,3 mg/ml injekčný roztok pre psy a mačky
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
Withdrawal period by route of administration:
  • Intramuscular use
    • Dog
    • Cat
  • Intravenous use
    • Dog
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN02AE01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Package description:
  • Clear glass vials type II, coated bromobutyl rubber stopper type I, aluminium cap, packed in a cardboard box. Package size: Cardboard box with 10 vials of 2 ml
  • Clear glass vials type II, coated bromobutyl rubber stopper type I, aluminium cap, packed in a cardboard box. Package size: Cardboard box with 3 vials of 2 ml
  • Clear glass vials type II, coated bromobutyl rubber stopper type I, aluminium cap, packed in a cardboard box. Package size: Cardboard box with 4 vials of 2 ml
  • Clear glass vials type II, coated bromobutyl rubber stopper type I, aluminium cap, packed in a cardboard box. Package size: Cardboard box with 5 vials of 2 ml
  • Clear glass vials type II, coated bromobutyl rubber stopper type I, aluminium cap, packed in a cardboard box. Package size: Cardboard box with 6 vials of 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:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/051/MR/18-S
Date of authorisation status change:
Reference member state:
  • Austria
Procedure number:
  • AT/V/0008/002
Concerned member states:
  • Bulgaria
  • Denmark
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Latvia
  • Lithuania
  • Norway
  • Portugal
  • Romania
  • Slovakia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

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Slovak (PDF)
Published on: 25/09/2023
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