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NARKAMON 50 mg/ml injekčný roztok

Authorised
  • Ketamine hydrochloride
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Product identification

Medicine name:
NARKAMON 50 mg/ml injekčný roztok
Active substance:
  • Ketamine hydrochloride
Target species:
  • Cattle (calf)
  • Sheep
  • Goat
  • Dog
  • Cat
  • Guinea pig
  • Monkey
  • Parrot
  • Reptile
  • Antelope
  • Roe deer
  • Pigeon
  • Red deer
  • Mouse
  • Rat
  • Horse
Route of administration:
  • Intramuscular use
  • Intraperitoneal use
  • Intravenous use

Product details

Active substance and strength:
  • Ketamine hydrochloride
    57.70
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle (calf)
      • Meat and offal
        24
        hour
    • Sheep
      • Meat and offal
        24
        hour
      • Milk
        0
        day
    • Goat
      • Meat and offal
        24
        hour
      • Milk
        0
        day
    • Dog
      • Not applicable
        0
        day
    • Cat
      • Not applicable
        0
        day
    • Guinea pig
      • Not applicable
        0
        day
    • Monkey
      • Not applicable
        0
        day
    • Parrot
      • Not applicable
        0
        day
    • Reptile
      • Not applicable
        0
        day
    • Antelope
      • Meat and offal
        24
        hour
    • Roe deer
      • Meat and offal
        24
        hour
    • Pigeon
      • Meat and offal
        24
        hour
    • Red deer
      • Meat and offal
        24
        hour
  • Intraperitoneal use
    • Mouse
      • Not applicable
        0
        day
    • Rat
      • Not applicable
        0
        day
  • Intravenous use
    • Horse
      • Meat and offal
        24
        hour
      • Milk
        0
        day
    • Dog
      • Not applicable
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01AX03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
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:
  • Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 99/172/88-C/S
Date of authorisation status change:

Documents

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Slovak (PDF)
Published on: 17/01/2022
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