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Veterinary Medicines

LUROCAINE

Authorised
  • Lidocaine hydrochloride monohydrate

Product identification

Medicine name:
LUROCAINE
Active substance:
  • Lidocaine hydrochloride monohydrate
Target species:
  • Dog
  • Cat
  • Equid
Route of administration:
  • Intramuscular use
  • Retrobulbar use
  • Subcutaneous use
  • Paravertebral use
  • Ocular use
  • Intravenous use
  • Intraperitoneal 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:
  • Intramuscular use
    • Dog
    • Cat
    • Equid
      • Milk
        3
        day
      • Meat and offal
        3
        day
  • Retrobulbar use
    • Dog
    • Cat
  • Subcutaneous use
    • Dog
    • Cat
  • Paravertebral use
    • Equid
      • Milk
        3
        day
      • Meat and offal
        3
        day
  • Ocular use
    • Dog
    • Cat
    • Equid
      • Milk
        3
        day
      • Meat and offal
        3
        day
  • Intravenous use
    • Dog
    • Cat
    • Equid
      • Milk
        3
        day
      • Meat and offal
        3
        day
  • Intraperitoneal use
    • Dog
    • Cat
    • Equid
      • Milk
        3
        day
      • Meat and offal
        3
        day
  • Intraarticular use
    • Equid
      • Milk
        3
        day
      • Meat and offal
        3
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01BB02
Authorisation status:
  • Valid
Authorised in:
  • France
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetoquinol Biowet Sp. z o.o.
  • Vetoquinol S.A.
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/9931286 6/1984
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 4/04/2022
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