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Veterinary Medicines

ANTOX 9 max

Authorised
  • Clostridium perfringens, type A, strain 28, toxoid
  • Clostridium perfringens, type C, beta toxoid
  • Clostridium perfringens, type D, strain 98, toxoid
  • Clostridium septicum, strain 1098, Inactivated
  • Clostridium novyi, type B, strain 34, toxoid
  • Clostridium novyi, strain 754, toxoid
  • Clostridium tetani, toxoid
  • Clostridium sordellii, toxoid

Identifikacija zdravila

Ime zdravila:
АНТОКС 9 макс
ANTOX 9 max
Učinkovina:
Pot uporabe:
  • Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:
  • Na voljo samo v English
    0.50
    international unit(s)
    /
    1.00
    Dose
  • Na voljo samo v English
    10.00
    international unit(s)
    /
    1.00
    Dose
  • Na voljo samo v English
    5.00
    international unit(s)
    /
    1.00
    Dose
  • Na voljo samo v English
    5.00
    billion colony forming units
    /
    1.00
    Dose
  • Na voljo samo v English
    6000.00
    Decimal potentisation
    /
    1.00
    Dose
  • Na voljo samo v English
    6000.00
    Decimal potentisation
    /
    1.00
    Dose
  • Na voljo samo v English
    1.00
    international unit(s)
    /
    1.00
    Dose
  • Na voljo samo v English
    1.00
    international unit(s)
    /
    1.00
    Dose
Farmacevtska oblika:
  • Suspenzija za injiciranje
Withdrawal period by route of administration:
  • Subcutaneous use
    • govedo
    • Sheep
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
  • QI02AB01
  • QI04AB01
Status dovoljenja:
  • Valid
Authorised in:
  • Bulgaria
Opis ovojnine:

Dodatne informacije

Entitlement type:
Imetnik dovoljenja za promet z zdravilom:
  • Mintech Co EOOD
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
  • Mintech Co EOOD
Pristojni organ:
  • BFSA
Številka dovoljenja :
  • 0022-3086
Datum spremembe statusa dovoljenja:

Dokumenti

Povzetek glavnih značilnosti zdravila

Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
Bulgarian (PDF)
Objavljeno na: 8/06/2022

Package Leaflet and Labelling

Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
Bulgarian (PDF)
Objavljeno na: 8/06/2022
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