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Veterinary Medicines

Euthadorm 500 mg/ml Injektionslösung

Odobreno
  • Pentobarbital sodium

Identifikacija proizvoda

Naziv lijeka:
Euthadorm 500 mg/ml Injektionslösung
Djelatna tvar:
Ciljne vrste:
Put aplikacije:

Pojedinosti o proizvodu

Djelatna tvar i jačina:
  • Dostupan samo u engleski
    500.00
    miligram
    /
    1.00
    mililitar
Farmaceutski oblik:
  • otopina za injekciju
Karencija prema putu aplikacije:
  • Intraperitonejski
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
  • Intravenski
    • Hare
      • Meat and offal
        no withdrawal period
    • Chicken
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Sheep
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
    • Pigeon
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
    • Goat
      • Meat and offal
        no withdrawal period
      • Milk
        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
  • U pluća
    • Chicken
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
    • Pigeon
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
Anatomsko-terapijsko-kemijska veterinarska (ATKvet) oznaka:
  • QN51AA01
Status odobrenja:
  • Važeće
Dostupan u:
  • Germany
Opis paketa:

Dodatne informacije

Vrsta prava:
  • Marketing Authorisation
Nositelj odobrenja za stavljanje u promet:
  • CP-Pharma Handelsgesellschaft mbH
Datum odobrenja za stavljanje u promet:
Mjesta proizvodnje za otpuštanje serije:
  • CP-Pharma Handelsgesellschaft mbH
Nadležno tijelo:
  • Federal Office Of Consumer Protection And Food Safety
Broj odobrenja:
  • 402340.00.00
Datum promjene statusa odobrenja:

Dokumenti

Combined File of all Documents

Ovaj dokument ne postoji na ovom jeziku (hrvatski). U nastavku ga možete pronaći na drugom jeziku.
njemački (PDF)
Objavljeno na: 2/09/2024

2402340-parde-20161220.pdf

njemački (PDF)
Objavljeno na: 3/01/2025
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