Lotagen Konzentrat

Ima dovoljenje za promet

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Informacije o zdravilu

Ime zdravila:

Lotagen Konzentrat

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

Pot uporabe:

Intracervikalna uporaba
Dermalna uporaba
Intrauterina uporaba
Intralezijska uporaba
Vaginalna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

360.00

milligram(s)

/

1.00

gram(s)

Farmacevtska oblika:

Koncentrat za dermalno raztopino

Karenca glede na pot uporabe:

Intracervikalna uporaba
- govedo
  - Meat and offal
    
    3
    
    day
  - Milk
    
    1
    
    day
- Sheep
  - Milk
    
    1
    
    day
  - Meat and offal
    
    3
    
    day
- Pig
  - Meat and offal
    
    3
    
    day
Dermalna uporaba
- govedo
  - Meat and offal
    
    3
    
    day
  - Milk
    
    1
    
    day
- Sheep
  - Milk
    
    1
    
    day
  - Meat and offal
    
    3
    
    day
- Horse
  - Milk
    
    1
    
    day
  - Meat and offal
    
    3
    
    day
- Pig
  - Meat and offal
    
    3
    
    day
Intrauterina uporaba
- govedo
  - Meat and offal
    
    3
    
    day
  - Milk
    
    1
    
    day
- Sheep
  - Milk
    
    1
    
    day
  - Meat and offal
    
    3
    
    day
- Horse
  - Milk
    
    1
    
    day
  - Meat and offal
    
    3
    
    day
- Pig
  - Meat and offal
    
    3
    
    day
Intralezijska uporaba
- govedo
  - Meat and offal
    
    3
    
    day
  - Milk
    
    1
    
    day
- Sheep
  - Milk
    
    1
    
    day
  - Meat and offal
    
    3
    
    day
- Horse
  - Milk
    
    1
    
    day
  - Meat and offal
    
    3
    
    day
- Pig
  - Meat and offal
    
    3
    
    day
Vaginalna uporaba
- govedo
  - Meat and offal
    
    3
    
    day
  - Milk
    
    1
    
    day
- Sheep
  - Milk
    
    1
    
    day
  - Meat and offal
    
    3
    
    day
- Horse
  - Milk
    
    1
    
    day
  - Meat and offal
    
    3
    
    day
- Pig
  - Meat and offal
    
    3
    
    day

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

QG51AD02

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:

Germany

Opis ovojnine zdravila:

Na voljo samo v German
Na voljo samo v German

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 Lithuanian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Intervet Deutschland GmbH

Datum dovoljenja za promet z zdravilom:

19/04/2005

Proizvodna mesta, odgovorna za sproščanje serij:

Trirx Segre

Pristojni organ:

Federal Office Of Consumer Protection And Food Safety

Številka dovoljenja za promet z zdravilom:

6174148.00.00

Datum spremembe statusa dovoljenja za promet:

19/04/2005

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

Dokumenti

Povzetek glavnih značilnosti zdravila

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

Drugi jeziki (1)

German (PDF)

Objavljeno na dan: 10/01/2025

Prenesi

Navodilo za uporabo

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

Drugi jeziki (1)

German (PDF)

Objavljeno na dan: 10/01/2025

Prenesi