ZINDEP 60 mg/ml injekčná suspenzia

Ni odobreno

Zinc
Zinc oxide

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Informacije o zdravilu

Ime zdravila:

ZINDEP 60 mg/ml injekčná suspenzia

Učinkovina:

Na voljo samo v English
Na voljo samo v English

Ciljne živalske vrste:

govedo
tele
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

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

40.00

milligram(s)

/

1.00

millilitre(s)
Na voljo samo v English

25.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Suspenzija za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- govedo
  - All relevant tissues
    
    no withdrawal period
    
    Without withdrawal period. The injection site and the surrounding area should be confiscated.
- tele
  - All relevant tissues
    
    no withdrawal period
    
    ithout withdrawal period. The injection site and the surrounding area should be confiscated.
- Sheep
  - All relevant tissues
    
    no withdrawal period
    
    ithout withdrawal period. The injection site and the surrounding area should be confiscated.
- Pig
  - All relevant tissues
    
    no withdrawal period
    
    ithout withdrawal period. The injection site and the surrounding area should be confiscated.

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

QA12CB

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Surrendered

Ima dovoljenje za promet v:

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

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:

BB Pharma a.s.

Datum dovoljenja za promet z zdravilom:

4/11/1991

Proizvodna mesta, odgovorna za sproščanje serij:

Farmacia Martin a.s.

Pristojni organ:

Institute For State Control Of Veterinary Biologicals And Medicaments

Številka dovoljenja za promet z zdravilom:

96/085/91-S

Datum spremembe statusa dovoljenja za promet:

11/11/2022

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

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