Veterinary Medicines

Vomend 5 mg/ml solution for injection for dogs and cats

Authorised
  • Metoclopramide hydrochloride
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Product identification

Medicine name:
Vomend 5 mg/ml solution for injection for dogs and cats
Vomend 5 mg/ml Injektionslösung für Hunde und Katzen
Active substance:
  • Metoclopramide hydrochloride
Target species:
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Metoclopramide hydrochloride
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Dog
    • Cat
  • Subcutaneous use
    • Dog
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA03FA01
Legal status of supply:
  • Medicinal product on medical prescription for renewable delivery
Authorisation status:
  • Valid
Authorised in:
  • Austria
Package description:
  • 50 ml vial of clear colourless glass type I. Bromobutyl rubber stoppers type I (the stoppers are secured with aluminium caps). 1 vial in a cardboard box.
  • 5 ml vial of clear colourless glass type I. Bromobutyl rubber stoppers type I (the stoppers are secured with aluminium caps). 1 vial in a cardboard box.
  • 10 ml vial of clear colourless glass type I. Bromobutyl rubber stoppers type I (the stoppers are secured with aluminium caps). 1 vial in a cardboard box.
  • 30 ml vial of clear colourless glass type I. Bromobutyl rubber stoppers type I (the stoppers are secured with aluminium caps). 1 vial in a cardboard box.
  • 25 ml vial of clear colourless glass type I. Bromobutyl rubber stoppers type I (the stoppers are secured with aluminium caps). 1 vial in a cardboard box.
  • 20 ml vial of clear colourless glass type I. Bromobutyl rubber stoppers type I (the stoppers are secured with aluminium caps). 1 vial in a cardboard box.

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:
  • Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Eurovet Animal Health B.V.
Responsible authority:
  • AGES
Authorisation number:
  • 8-00913
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0145/001
Concerned member states:
  • Austria
  • Belgium
  • Germany
  • Italy
  • Luxembourg
  • Portugal
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 23/12/2015
Updated on: 23/03/2022
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Summary of Product Characteristics

English (PDF)
Published on: 16/06/2022
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German (PDF)
Published on: 23/12/2015
Updated on: 23/03/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 23/12/2015
Updated on: 23/03/2022
Download

106887 par.pdf

English (PDF)
Published on: 16/06/2022
Download
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