Veterinary Medicines

Buprecare Multidose 0.3 mg/ml Solution for Injection for Dogs and Cats

Authorised
  • Buprenorphine hydrochloride
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Product identification

Medicine name:
Buprecare Multidose 0.3 mg/ml Solution for Injection for Dogs and Cats
Buprecare Multidose 0,3 mg/ml raztopina za injiciranje za pse in mačke
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:
  • Slovenia
Package description:
  • Presented in a 10 ml amber Type I glass vial with a bromobutyl rubber stopper and flip-off aluminium cap.Pack size: 1 vial with 10 ml solution for injection.

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:
  • Ecuphar
Marketing authorisation date:
This information is not available for this product.
Manufacturing sites for batch release:
  • Produlab Pharma B.V.
Responsible authority:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • MR/V/0622/001
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0453/002
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • France
  • Germany
  • Greece
  • Hungary
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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Slovenian (PDF)
Published on: 23/02/2022
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Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 23/02/2022
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