Veterinary Medicines

LUROCAINE

Authorised
  • Lidocaine hydrochloride monohydrate
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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
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Dog
    • Cat
    • Equid
      • Meat and offal, milk
        3
        day
  • Retrobulbar use
    • Dog
    • Cat
    • Equid
      • Meat and offal, milk
        3
        day
  • Subcutaneous use
    • Dog
    • Cat
    • Equid
      • Meat and offal, milk
        3
        day
  • Paravertebral use
    • Dog
    • Cat
    • Equid
      • Meat and offal, milk
        3
        day
  • Ocular use
    • Dog
    • Cat
    • Equid
      • Meat and offal, milk
        3
        day
  • Intravenous use
    • Dog
    • Cat
    • Equid
      • Meat and offal, milk
        3
        day
  • Intraperitoneal use
    • Dog
    • Cat
    • Equid
      • Meat and offal, milk
        3
        day
  • Intraarticular use
    • Dog
    • Cat
    • Equid
      • Meat and offal, 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:
  • Luxembourg
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetoquinol S.A.
Responsible authority:
  • Ministry Of Health And Social Security
Authorisation number:
  • V 808/09/07/1225
Date of authorisation status change:

Documents

Summary of Product Characteristics

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French (PDF)
Published on: 25/03/2024
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