Veterinary Medicine Information website

Narketan 10 oplossing voor injectie

Odobreno
  • Ketamine hydrochloride
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Identifikacija proizvoda

Naziv lijeka:
Narketan 10 oplossing voor injectie
Djelatna tvar:
Ciljne vrste:
Put aplikacije:
  • Intramuskularno
  • Intravenski

Pojedinosti o proizvodu

Djelatna tvar i jačina:
  • Dostupan samo u engleski
    115.34
    miligram
    /
    1.00
    mililitar
Farmaceutski oblik:
  • otopina za injekciju
Karencija prema putu aplikacije:
  • Intramuskularno
    • Cattle
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Goat (adult female)
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Sheep
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
    • Cattle (calf)
      • Meat and offal
        no withdrawal period
      • Meat and offal
        no withdrawal period
  • Intravenski
    • Cattle
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Goat (adult female)
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Sheep
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
    • Cattle (calf)
      • Meat and offal
        no withdrawal period
      • Meat and offal
        no withdrawal period
Anatomsko-terapijsko-kemijska veterinarska (ATKvet) oznaka:
  • QN01AX03
Pravni status opskrbe:
Status odobrenja:
  • Važeće
Odobreno u:
Dostupan u:
  • Netherlands
Opis paketa:

Dodatne informacije

Vrsta prava:
  • Marketing Authorisation
Pravna osnova za odobrenje proizvoda:
Nositelj odobrenja za stavljanje u promet:
  • Vetoquinol B.V.
Datum odobrenja za stavljanje u promet:
Mjesta proizvodnje za otpuštanje serije:
  • Vétoquinol SA
Nadležno tijelo:
  • Medicines Evaluation Board
Broj odobrenja:
  • REG NL 2403
Datum promjene statusa odobrenja:

Dokumenti

Combined File of all Documents

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nizozemski (PDF)
Objavljeno na: 15/02/2022
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