Veterinary Medicines

LIDOR 20 MG/ML SOLUTION FOR INJECTION FOR HORSES, DOGS AND CATS

Authorised
  • Lidocaine hydrochloride monohydrate
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Product identification

Medicine name:
LIDOR 20 MG/ML SOLUTION FOR INJECTION FOR HORSES, DOGS AND CATS
Lidor vet. 20 mg/ml injektioneste, liuos
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 monohydrate
    24.65
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Epidural use
    • Dog
    • Cat
    • Horse
      • Meat and offal
        3
        day
      • Milk
        3
        day
  • Subcutaneous use
    • Dog
    • Cat
    • Horse
      • Meat and offal
        3
        day
      • Milk
        3
        day
  • Perineural use
    • Dog
    • Cat
    • Horse
      • Meat and offal
        3
        day
      • Milk
        3
        day
  • Ocular use
    • Dog
    • Cat
    • Horse
      • Meat and offal
        3
        day
      • Milk
        3
        day
  • Intraarticular use
    • Dog
    • Cat
    • Horse
      • Meat and offal
        3
        day
      • Milk
        3
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01BB02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Finland
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:
  • Finnish Medicines Agency
Authorisation number:
  • 34971
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
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