Veterinary Medicines

Narketan 100 mg/ml - Injektionslösung für Tiere

Authorised
  • Ketamine hydrochloride
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Product identification

Medicine name:
Narketan 100 mg/ml - Injektionslösung für Tiere
Active substance:
  • Ketamine hydrochloride
Target species:
  • Reptile
  • Birds
  • Cattle (calf)
  • Dog
  • Goat
  • Sheep
  • Cat
  • Rabbit
  • Guinea pig
  • Hamster
  • Pig
  • Wild animals
  • Cattle
  • Horse
Route of administration:
  • Intramuscular use
  • Intraperitoneal use
  • Intravenous use
  • Subcutaneous 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
    • Reptile
    • Birds
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Dog
    • Goat
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Cat
    • Rabbit
      • Meat and offal
        0
        day
    • Guinea pig
    • Hamster
    • Pig
      • Meat and offal
        0
        day
    • Wild animals
      • Meat and offal
        0
        day
  • Intraperitoneal use
    • Reptile
  • Intravenous use
    • Cattle
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Dog
    • Goat
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Horse
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Rabbit
      • Meat and offal
        0
        day
    • Guinea pig
    • Hamster
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01AX03
Legal status of supply:
  • Medicinal product on medical prescription for non-renewable delivery
Authorisation status:
  • Valid
Authorised in:
  • Austria
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Vetoquinol Oesterreich GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • VETOQUINOL SA
Responsible authority:
  • AGES
Authorisation number:
  • 8-00223
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 11/01/2021
Download

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 11/12/2020
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 24/01/2019
Download
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