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Veterinary Medicines

Narkodorm 200 mg/ml Injektionslösung

Ima dovoljenje za promet
  • Pentobarbital sodium

Informacije o zdravilu

Ime zdravila:
Narkodorm 200 mg/ml Injektionslösung
Učinkovina:
Ciljne živalske vrste:
Pot uporabe:
  • Intravenska uporaba
  • Intrakardialna uporaba
  • Intrapulmonalna uporaba
  • Intraperitonealna uporaba

Podatki o zdravilu

Učinkovina / Jakost:
  • Na voljo samo v English
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
Farmacevtska oblika:
  • Raztopina za injiciranje
Karenca glede na pot uporabe:
  • Intravenska uporaba
    • 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
  • Intrakardialna uporaba
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
  • Intrapulmonalna uporaba
    • Chicken
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
    • Pigeon
      • Egg
        no withdrawal period
      • Meat and offal
        no withdrawal period
  • Intraperitonealna uporaba
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):
  • QN05CA01
Status dovoljenja za promet z zdravilom:
  • Valid
Na voljo v:
  • Germany
Opis ovojnine zdravila:

Dodatne informacije

Imetnik dovoljenja za promet z zdravilom:
  • CP-Pharma Handelsgesellschaft mbH
Datum dovoljenja za promet z zdravilom:
Proizvodna mesta, odgovorna za sproščanje serij:
  • CP-Pharma Handelsgesellschaft mbH
Pristojni organ:
  • Federal Office Of Consumer Protection And Food Safety
Številka dovoljenja za promet z zdravilom:
  • 402465.00.00
Datum spremembe statusa dovoljenja za promet:

Dokumenti

Combined File of all Documents

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German (PDF)
Objavljeno na dan: 3/01/2025

2402465-parde-20181108-k.pdf

German (PDF)
Objavljeno na dan: 3/01/2025
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