TERRAMYCIN LA

Ima dovoljenje za promet

Oxytetracycline

Prenes kot PDF

Informacije o zdravilu

Ime zdravila:

TERRAMYCIN LA

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

Pot uporabe:

intramuskularna uporaba
Intravenska uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

200.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- govedo
  - Meat and offal
    
    21
    
    day
  - Milk
    
    7
    
    day
- Sheep
  - Meat and offal
    
    21
    
    day
    
    Nu se va administra la oile producătoare de lapte destinat consumului uman
- Pig
  - Meat and offal
    
    21
    
    day
- Red deer
  - Meat and offal
    
    30
    
    day
Intravenska uporaba
- govedo
  - Meat and offal
    
    21
    
    day
  - Milk
    
    72
    
    hour
- Sheep
  - Meat and offal
    
    21
    
    day
Subkutana uporaba
- brojler
  - Meat and offal
    
    0
    
    day
    
    Nu se va administra la păsările ce produc ouă destinate consumului uman.

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 Lithuanian Dutch Portuguese Romanian Slovak Swedish Icelandic Norwegian

Na voljo v:

Romania

Opis ovojnine zdravila:

Na voljo samo v Romanian
Na voljo samo v Romanian
Na voljo samo v Romanian
Na voljo samo v Romanian
Na voljo samo v Romanian

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

Imetnik dovoljenja za promet z zdravilom:

Zoetis Belgium

Datum dovoljenja za promet z zdravilom:

22/06/2006

Proizvodna mesta, odgovorna za sproščanje serij:

Zoetis Manufacturing & Research Spain, S.L.

Pristojni organ:

Institute For Control Of Biological Products And Veterinary Medicines

Številka dovoljenja za promet z zdravilom:

140027

Datum spremembe statusa dovoljenja za promet:

5/12/2024

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

Dokumenti

Combined File of all Documents

Ta dokument ne obstaja v tem jeziku (slovenščina). Lahko ga najdete spodaj v drugem jeziku.

Drugi jeziki (1)

Romanian (PDF)

Objavljeno na dan: 12/12/2024

Prenesi