Veterinary Medicine Information website

Rococlos Vet. injektionsvæske, emulsion

Odobreno
  • Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
  • Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated
  • Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated
  • Porcine rotavirus A, strain OSU 6, Inactivated
  • Porcine rotavirus A, strain OSU 6, Inactivated
  • Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
  • Clostridium perfringens, type C, beta toxoid
  • Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
  • Clostridium perfringens, type C, beta toxoid
  • Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
  • Clostridium perfringens, type C, beta toxoid
  • Porcine rotavirus A, strain OSU 6, Inactivated
  • Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
  • Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
  • Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
  • Porcine rotavirus A, strain OSU 6, Inactivated
  • Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
  • Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated
  • Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated
  • Clostridium perfringens, type C, beta toxoid
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Identifikacija proizvoda

Naziv lijeka:
Rococlos Vet. injektionsvæske, emulsion
Djelatna tvar:
Ciljne vrste:
Put aplikacije:
  • Intramuskularno

Pojedinosti o proizvodu

Djelatna tvar i jačina:
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
  • Dostupan samo u engleski
    1.00
    relative potency
    /
    1.00
    Dose
Farmaceutski oblik:
  • emulzija za injekciju
Karencija prema putu aplikacije:
  • Intramuskularno
    • Pig
      • Meat
        0
        day
      • Meat
        0
        day
      • Meat
        0
        day
      • Meat
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        day
      • Meat
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        day
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        day
      • Meat
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        day
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      • Meat
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        day
      • Meat
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      • Meat
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      • Meat
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      • Meat
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      • Meat
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      • Meat
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      • Meat
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        day
      • Meat
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        day
      • Meat
        0
        day
      • Meat
        0
        day
      • Meat
        0
        day
Pravni status opskrbe:
Status odobrenja:
  • Važeće
Odobreno u:
Dostupan u:
  • Denmark
Opis paketa:

Dodatne informacije

Vrsta prava:
Pravna osnova za odobrenje proizvoda:
Nositelj odobrenja za stavljanje u promet:
  • Salfarm Danmark A/S
Datum odobrenja za stavljanje u promet:
Mjesta proizvodnje za otpuštanje serije:
  • Bioveta a.s.
Nadležno tijelo:
  • Danish Medicines Agency
Broj odobrenja:
  • 72024
Datum promjene statusa odobrenja:

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danski (, INJEKTIONSVÆSKE, EMULSION)
Objavljeno na: 24/06/2026
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