NARCOREN
  • Pentobarbitalnatrium
  • Valid
Authorised in these countries:
  • Germany
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Identifikacija zdravila

Ime zdravila:
NARCOREN
Učinkovina / Jakost:
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
  • QN05CA01
  • QN51AA
Številka dovoljenja :
  • 6088986.00.00
Identifikacijska številka zdravila:
  • 75d7a814-15ae-4bc3-a6e5-01c78db8bb6b
Stalna identifikacijska številka:
  • 600000072823

Podatki o zdravilu

Pravni status za dobavo / izdajo zdravila:
  • Zdravilo, ki se izdaja na veterinarski recept
Farmacevtska oblika:
  • Raztopina za injiciranje
Withdrawal period by route of administration:
  • Intravenous use
    • Hamster
    • Hare
      • Meat and offal
        no withdrawal period
    • Chicken
      • Egg
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Dog
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Cat
    • Mouse
    • Guinea pig
    • Horse
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Rat
    • Pigeon
      • Egg
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • okrasna ptica
  • Intraperitoneal use
    • Lizard
    • Hamster
    • Hare
      • Meat and offal
        no withdrawal period
    • Chicken
      • Egg
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Dog
    • Polecat
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Cat
    • Mouse
    • Guinea pig
    • Mink
    • Rat
    • Turtle
    • Snake
    • Pigeon
      • Egg
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • okrasna ptica
    • Frog

Razpoložljivost

Opis ovojnine:
Proizvodna mesta, odgovorna za sproščanje serij:
Ta podatek za to zdravilo ni na voljo.
Source wholesaler:
Ta podatek za to zdravilo ni na voljo.
Destination wholesaler:
Ta podatek za to zdravilo ni na voljo.

Podatki o dovoljenju za promet

Status dovoljenja:
Vrsta postopka za pridobitev dovoljenja:
Številka postopka:
  • 0088986
Datum spremembe statusa dovoljenja:
Pravna podlaga za izdajo dovoljenja za promet z zdravilom:
Država izdaje dovoljenja:
Pristojni organ:
  • BVL
Imetnik dovoljenja za promet z zdravilom:
  • Boehringer Ingelheim Vetmedica GmbH
Izdano dovoljenje za promet z zdravilom:
Referenčna država članica:
Ta podatek za to zdravilo ni na voljo.
Zadevne države članice:
Ta podatek za to zdravilo ni na voljo.
Oznaka referenčnega zdravila:
Ta podatek za to zdravilo ni na voljo.
Oznaka izvornega zdravila:
Ta podatek za to zdravilo ni na voljo.

Dodatne informacije

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

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