Insistor 10 mg/ml solution for injection for dogs and cats
Insistor 10 mg/ml solution for injection for dogs and cats
Authorised
- Methadone hydrochloride
Product identification
Medicine name:
Insistor 10 mg/ml solution for injection for dogs and cats
Insistor 10 mg/ml ενέσιμο διάλυμα για σκύλους και γάτες
Active substance:
- Methadone hydrochloride
Target species:
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Methadone hydrochloride10.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN02AC90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Available in:
-
Greece
Package description:
- Clear glass vial with grey, coated chlorobutyl rubber stopper and aluminium pull off cap or aluminium/plastic flip off cap. Package size 1x 5 ml
- Clear glass vial with grey, coated chlorobutyl rubber stopper and aluminium pull off cap or aluminium/plastic flip off cap. Package size 5x 10 ml
- Clear glass vial with grey, coated chlorobutyl rubber stopper and aluminium pull off cap or aluminium/plastic flip off cap. Package size 5 x 5 ml
- Clear glass vial with grey, coated chlorobutyl rubber stopper and aluminium pull off cap or aluminium/plastic flip off cap. Package size 1x 10 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:
- National Organization For Medicines
Authorisation number:
- 42691-19/05/2021-Κ-0246301
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0235/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Greek (PDF)
Published on: 4/09/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Greek (PDF)
Published on: 4/09/2025
Combined File of all Documents
English (PDF)
Download Published on: 16/05/2025