ACTI-TETRA I

Ima dovoljenje za promet

Oxytetracycline hydrochloride

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Informacije o zdravilu

Ime zdravila:

ACTI-TETRA I

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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

intramuskularna uporaba
Subkutana uporaba
Intravenska uporaba
Intraperitonealna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

53.96

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- govedo
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Pig
  - Meat and offal
    
    14
    
    day
- Horse
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Sheep
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Goat
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
Subkutana uporaba
- govedo
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Pig
  - Meat and offal
    
    14
    
    day
- Horse
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Sheep
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Goat
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
Intravenska uporaba
- govedo
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Pig
  - Meat and offal
    
    14
    
    day
- Horse
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Sheep
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
    
    .
- Goat
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
Intraperitonealna uporaba
- govedo
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Pig
  - Meat and offal
    
    14
    
    day
- Horse
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Sheep
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day
- Goat
  - Milk
    
    3
    
    day
  - Meat and offal
    
    14
    
    day

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

QJ01AA06

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:

Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian

Na voljo v:

France

Opis ovojnine zdravila:

Na voljo samo v French
Na voljo samo v French

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:

Laboratoires Biove

Datum dovoljenja za promet z zdravilom:

6/05/1988

Proizvodna mesta, odgovorna za sproščanje serij:

LABORATOIRES BIOVE

Pristojni organ:

French Agency For Food, Environmental And Occupational Health & Safety

Številka dovoljenja za promet z zdravilom:

FR/V/6090637 3/1988

Datum spremembe statusa dovoljenja za promet:

6/05/2013

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

Dokumenti

Povzetek glavnih značilnosti zdravila

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