Veterinary Medicine Information website

Penbital Eutha, 400mg/ml, Injekční roztok

Odobreno
  • Pentobarbital

Identifikacija proizvoda

Naziv lijeka:
Penbital Eutha, 400mg/ml, Injekční roztok
Djelatna tvar:
Ciljne vrste:
Put aplikacije:
  • U pluća
  • Intravenski
  • Intrakardijalno
  • Intraperitonejski

Pojedinosti o proizvodu

Djelatna tvar i jačina:
  • Dostupan samo u engleski
    362.94
    miligram
    /
    1.00
    mililitar
Farmaceutski oblik:
  • otopina za injekciju
Karencija prema putu aplikacije:
  • U pluća
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Chicken
      • Meat and offal
        no withdrawal period
    • Pigeon
      • Meat and offal
        no withdrawal period
    • Ornamental bird
      • Meat and offal
        no withdrawal period
  • Intravenski
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Chicken
      • Meat and offal
        no withdrawal period
    • Pigeon
      • Meat and offal
        no withdrawal period
    • Ornamental bird
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
    • Horse (pony)
      • Meat and offal
        no withdrawal period
    • Cattle
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
  • Intrakardijalno
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
  • Intraperitonejski
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Frog
      • Meat and offal
        no withdrawal period
Anatomsko-terapijsko-kemijska veterinarska (ATKvet) oznaka:
  • QN51AA01
Status odobrenja:
  • Važeće
Opis paketa:

Dodatne informacije

Vrsta prava:
  • Marketing Authorisation
Nositelj odobrenja za stavljanje u promet:
  • Bioveta a.s.
Datum odobrenja za stavljanje u promet:
Mjesta proizvodnje za otpuštanje serije:
  • Bioveta a.s.
Nadležno tijelo:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Broj odobrenja:
  • 96/014/21-C
Datum promjene statusa odobrenja:

Dokumenti

Sažetak opisa svojstava lijeka

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češki (PDF)
Objavljeno na: 5/05/2026

Uputa o lijeku

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češki (PDF)
Objavljeno na: 26/10/2022

Označivanje

Ovaj dokument ne postoji na ovom jeziku (hrvatski). Možete ga pronaći na drugom jeziku ispod.
češki (PDF)
Objavljeno na: 26/10/2022