Butomidor 10 mg/ml Roztwór do wstrzykiwań

Ima dovoljenje za promet

Butorphanol

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Informacije o zdravilu

Ime zdravila:

Butomidor 10 mg/ml Roztwór do wstrzykiwań

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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
Intravenska uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- Horse
  - All relevant tissues
    
    no withdrawal period
    
    Not to be used in animals intended for human consumption.
    Treated horses may never be slaughtered for human consumption.
    The horse must have been declared as not intended for human consumption under national horse passport legislation.
Intravenska uporaba
- Horse
  - All relevant tissues
    
    no withdrawal period
    
    Not to be used in animals intended for human consumption.
    Treated horses may never be slaughtered for human consumption.
    The horse must have been declared as not intended for human consumption under national horse passport legislation.
Subkutana uporaba
- Horse
  - All relevant tissues
    
    no withdrawal period
    
    Not to be used in animals intended for human consumption.
    Treated horses may never be slaughtered for human consumption.
    The horse must have been declared as not intended for human consumption under national horse passport legislation.

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

QN02AF01

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:

Poland

Opis ovojnine zdravila:

Na voljo samo v Polish

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 Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Vetviva Richter GmbH

Datum dovoljenja za promet z zdravilom:

19/12/2001

Proizvodna mesta, odgovorna za sproščanje serij:

Vetviva Richter GmbH

Pristojni organ:

Office For Registration Of Medicinal Products Medical Devices And Biocidal Products

Številka dovoljenja za promet z zdravilom:

1236

Datum spremembe statusa dovoljenja za promet:

19/12/2001

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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Navodilo za uporabo

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

Drugi jeziki (1)

Polish (PDF)

Objavljeno na dan: 4/02/2022

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