FATROXIMIN 300 mg intrauterinné tablety

Ima dovoljenje za promet

Rifaximin

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Informacije o zdravilu

Ime zdravila:

FATROXIMIN 300 mg intrauterinné tablety

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

krava
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Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian

Pot uporabe:

Vaginalna uporaba
Intrauterina uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

300.00

milligram(s)

/

1.00

Tableta

Farmacevtska oblika:

intrauterina tableta

Karenca glede na pot uporabe:

Vaginalna uporaba
- krava
  - Milk
    
    0
    
    day
    
    Milk: zero hours.
  - Meat and offal
    
    0
    
    day
    
    Meat and offal: zero days.
- Buffalo (female)
  - Milk
    
    0
    
    day
    
    Milk: zero hours.
  - Meat and offal
    
    0
    
    day
    
    Meat and offal: zero days.
- Horse (mare)
  - Milk
    
    0
    
    day
    
    Milk: zero hours.
  - Meat and offal
    
    0
    
    day
    
    Meat and offal: zero days. Do not use in mares whose meat is intended for human consumption.
Intrauterina uporaba
- krava
  - Meat and offal
    
    0
    
    day
    
    Meat and offal: zero days.
  - Milk
    
    0
    
    day
    
    Milk: zero hours.
- Horse (mare)
  - Meat and offal
    
    0
    
    day
    
    Meat and offal: zero days. Do not use in mares whose meat is intended for human consumption.
  - Milk
    
    0
    
    day
    
    Milk: 0 hours.
- Buffalo (female)
  - Meat and offal
    
    0
    
    day
    
    Meat and offal: zero days.
  - Milk
    
    0
    
    day
    
    Milk: zero hours.

Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):

QG51AA06

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Valid

Ima dovoljenje za promet v:

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Na voljo v:

Slovakia

Opis ovojnine zdravila:

Na voljo samo v Slovak
Na voljo samo v Slovak

Dodatne informacije

Vrsta dovoljenja:

Na voljo samo v English French Croatian Italian Latvian Finnish Swedish Icelandic Norwegian

Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English French Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Fatro S.p.A.

Datum dovoljenja za promet z zdravilom:

23/12/1997

Proizvodna mesta, odgovorna za sproščanje serij:

Fatro S.p.A.

Pristojni organ:

Institute For State Control Of Veterinary Biologicals And Medicaments

Številka dovoljenja za promet z zdravilom:

96/0637/97-S

Datum spremembe statusa dovoljenja za promet:

23/12/1997

Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet

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Objavljeno na dan: 14/12/2021

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