Veterinary Medicines

Diazedor 5 mg/ml Injektionslösung für Hunde und Katzen

Authorised
  • Diazepam
  • Diazepam
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Product identification

Medicine name:
Diazedor 5 mg/ml Injektionslösung für Hunde und Katzen
Diazedor 5 mg/ml soluzione iniettabile per cani e gatti
Active substance:
  • Diazepam
  • Diazepam
Target species:
  • Dog
  • Cat
  • Dog
  • Cat
Route of administration:
  • Intravenous use
  • Intravenous use

Product details

Active substance and strength:
  • Diazepam
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Diazepam
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN05BA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Available in:
  • Italy
Package description:
  • Colourless glass ampoules, type I, with 2 ml solution for injection, closed with a chlorobutyl rubber stopper and either an aluminium pull off cap or an aluminium/plastic flip off cap. Pack size: 10 x 2 ml in a cardboard box.
  • Colourless glass ampoules, type I, with 2 ml solution for injection, closed with a chlorobutyl rubber stopper and either an aluminium pull off cap or an aluminium/plastic flip off cap. Pack size: 5 x 2 ml in a cardboard box.
  • Colourless glass vials, type I, with 10 ml solution for injection, closed with a chlorobutyl rubber stopper and either an aluminium pull off cap or an aluminium/plastic flip off cap. Pack size: 1 x 10 ml in a cardboard box.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetviva Richter GmbH
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 105132
Date of authorisation status change:
Reference member state:
  • Austria
Procedure number:
  • AT/V/0017/001
Concerned member states:
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)
Generic of:

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 16/11/2023
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Summary of Product Characteristics

English (PDF)
Published on: 13/03/2025
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