Vomend 5 mg/ml solution for injection for dogs and cats
Vomend 5 mg/ml solution for injection for dogs and cats
Authorised
- Metoclopramide hydrochloride
Product identification
Medicine name:
Vomend 5 mg/ml solution for injection for dogs and cats
Vomend Anti-Emeticum 5 mg/ml Oplossing voor injectie
Vomend Anti-Emeticum 5 mg/ml Solution injectable
Vomend Anti-Emeticum 5 mg/ml Injektionslösung
Active substance:
- Metoclopramide hydrochloride
Target species:
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Metoclopramide hydrochloride5.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA03FA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
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:
- Dechra Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Eurovet Animal Health B.V.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V381805
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)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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106887 par.pdf
English (PDF)
Download Published on: 16/06/2022
