LIDOR 20 MG/ML SOLUTION FOR INJECTION FOR HORSES, DOGS AND CATS
LIDOR 20 MG/ML SOLUTION FOR INJECTION FOR HORSES, DOGS AND CATS
Authorised
- Lidocaine hydrochloride monohydrate
Product identification
Medicine name:
LIDOR 20 MG/ML SOLUTION FOR INJECTION FOR HORSES, DOGS AND CATS
Lidor 20 mg/ml Oplossing voor injectie
Lidor 20 mg/ml Solution injectable
Lidor 20 mg/ml Injektionslösung
Active substance:
- Lidocaine hydrochloride monohydrate
Target species:
-
Dog
-
Cat
-
Horse
Route of administration:
-
Epidural use
-
Subcutaneous use
-
Perineural use
-
Ocular use
-
Intraarticular use
Product details
Active substance and strength:
-
Lidocaine hydrochloride monohydrate24.65milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Epidural use
- Dog
- Cat
- Horse
-
Meat and offal3day
-
Milk3day
-
-
Subcutaneous use
- Dog
- Cat
- Horse
-
Meat and offal3day
-
Milk3day
-
-
Perineural use
- Dog
- Cat
- Horse
-
Meat and offal3day
-
Milk3day
-
-
Ocular use
- Dog
- Cat
- Horse
-
Meat and offal3day
-
Milk3day
-
-
Intraarticular use
- Dog
- Cat
- Horse
-
Meat and offal3day
-
Milk3day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN01BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- 5 x 50 ml vials
- 100 ml vial
- 5 x 100 ml vials
- 250 ml vial
- 50 ml vial
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:
- Richter Pharma AG
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetviva Richter GmbH
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V525386
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0318/001
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Germany
-
Iceland
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Spain
-
Sweden
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.
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
How useful was this page?: