Veterinary Medicines

BOVALTO TRIVACTON 6

Ni odobreno
  • Escherichia coli, serotype O101 (fimbrial adhesin F41), Inactivated
  • Escherichia coli, serotype O78 (antigen 31A), Inactivated
  • Escherichia coli, serotype O101 (fimbrial adhesin F5), Inactivated
  • Bovine coronavirus, strain INRA, Inactivated
  • Escherichia coli, serotype O117 (antigen Y), Inactivated
  • Bovine rotavirus A, Inactivated
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Informacije o zdravilu

Ime zdravila:
BOVALTO TRIVACTON 6
Učinkovina:
Ciljne živalske vrste:
  • govedo
Pot uporabe:
  • Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:
  • Na voljo samo v English
    0.90
    log10 serum neutralising unit(s)
    /
    1.00
    millilitre(s)
  • Na voljo samo v English
    0.90
    log10 serum neutralising unit(s)
    /
    1.00
    millilitre(s)
  • Na voljo samo v English
    0.90
    log10 serum neutralising unit(s)
    /
    1.00
    millilitre(s)
  • Na voljo samo v English
    1.50
    log10 serum neutralising unit(s)
    /
    1.00
    millilitre(s)
  • Na voljo samo v English
    0.90
    log10 serum neutralising unit(s)
    /
    1.00
    millilitre(s)
  • Na voljo samo v English
    2.00
    log10 haemagglutination inhibiting unit(s)
    /
    1.00
    millilitre(s)
Farmacevtska oblika:
  • Suspenzija za injiciranje
Karenca glede na pot uporabe:
  • Subkutana uporaba
    • govedo
      • Milk
        0
        day
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      • Milk
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      • Milk
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      • Meat and offal
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      • Milk
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      • Meat and offal
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        day
    • govedo
      • Milk
        0
        day
      • Meat and offal
        0
        day
      • Milk
        0
        day
      • Meat and offal
        0
        day
      • Milk
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      • Milk
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      • Milk
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      • Milk
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Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):
  • QI02AL01
Pravni status za dobavo/izdajo zdravila:
  • Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja za promet z zdravilom:
  • Surrendered
Ima dovoljenje za promet v:
Opis ovojnine zdravila:

Dodatne informacije

Vrsta dovoljenja:
Pravna podlaga za izdajo dovoljenja za promet z zdravilom:
Imetnik dovoljenja za promet z zdravilom:
  • Boehringer Ingelheim Animal Health Italia S.p.A. In Breve Boehringer Ingelheim Ah It S.p.A.
Datum dovoljenja za promet z zdravilom:
Proizvodna mesta, odgovorna za sproščanje serij:
  • Boehringer Ingelheim Animal Health France
Pristojni organ:
  • Ministry Of Health
Številka dovoljenja za promet z zdravilom:
Ta podatek za to zdravilo ni na voljo.
Datum spremembe statusa dovoljenja za promet:

Dokumenti

Combined File of all Documents

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Italian (PDF)
Objavljeno na dan: 7/03/2023
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