Veterinary Medicines

Narkodorm 200 mg/ml Injektionslösung

Authorised
  • Pentobarbital sodium
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Product identification

Medicine name:
Narkodorm 200 mg/ml Injektionslösung
Active substance:
  • Pentobarbital sodium
Target species:
  • Pigeon
  • Chicken
  • Ornamental bird
  • Dog
  • Horse
  • Horse (pony)
  • Cat
  • Hare
  • Rabbit
  • Mink
  • Polecat
  • Guinea pig
  • Hamster
  • Mouse
  • Rat
  • Frog
  • Lizard
  • Snake
  • Turtle
Route of administration:
  • Intravenous use
  • Intracardiac use
  • Intrapulmonary use
  • Intraperitoneal use

Product details

Active substance and strength:
  • Pentobarbital sodium
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Pigeon
      • Egg
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Chicken
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Horse (pony)
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
  • Intracardiac use
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
  • Intrapulmonary use
    • Chicken
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
    • Pigeon
      • Egg
        no withdrawal period
      • Meat and offal
        no withdrawal period
  • Intraperitoneal use
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN05CA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • CP-Pharma Handelsgesellschaft mbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • CP-Pharma Handelsgesellschaft mbH
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 402465.00.00
Date of authorisation status change:

Documents

Combined File of all Documents

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German (PDF)
Published on: 3/01/2025
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2402465-parde-20181108-k.pdf

German (PDF)
Published on: 3/01/2025
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