Veterinary Medicines

Narketan 10 oplossing voor injectie

Authorised
  • Ketamine hydrochloride
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Product identification

Medicine name:
Narketan 10 oplossing voor injectie
Active substance:
  • Ketamine hydrochloride
Target species:
  • Cattle
  • Goat (adult female)
  • Sheep
  • Horse
  • Pig
  • Cattle (calf)
  • Ornamental bird
  • Homing pigeon
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Ketamine hydrochloride
    115.34
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Goat (adult female)
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Sheep
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
    • Cattle (calf)
      • Meat and offal
        no withdrawal period
      • Meat and offal
        no withdrawal period
  • Intravenous use
    • Cattle
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Goat (adult female)
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Sheep
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
    • Cattle (calf)
      • Meat and offal
        no withdrawal period
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01AX03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Available in:
  • Netherlands
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 B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vétoquinol SA
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 2403
Date of authorisation status change:

Documents

Combined File of all Documents

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Dutch (PDF)
Published on: 15/02/2022
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