Veterinary Medicine Information website

Clindabactin 55 mg žvečljive tablete za pse in mačke

Ima dovoljenje za promet

Clindamycin hydrochloride

Informacije o zdravilu

Ime zdravila:

Clindabactin 55 mg žvečljive tablete za pse in mačke

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

Pot uporabe:

Peroralna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

55.00

milligram(s)

/

1.00

Tableta

Farmacevtska oblika:

Žvečljiva tableta

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

QJ01FF01

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:

Slovenia

Opis ovojnine zdravila:

Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla s 5 pretisnimi omoti s po 10 tabletami.
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla s 4 pretisnimi omoti s po 10 tabletami.
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla s 3 pretisnimi omoti s po 10 tabletami.
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla s 25 pretisnimi omoti s po 10 tabletami
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla z 2 pretisnimi omoti s po 10 tabletami.
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla z 10 pretisnimi omoti s po 10 tabletami.
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla, ki vsebuje 10 ločenih škatel, ki vsaka vsebuje 1 pretisni omot z 10 tabletami.
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla z 9 pretisnimi omoti s po 10 tabletami.
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla z 8 pretisnimi omoti s po 10 tabletami.
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla s 7 pretisnimi omoti s po 10 tabletami.
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla s 6 pretisnimi omoti s po 10 tabletami.
Aluminij-poliamid/aluminij/PVC pretisni omoti Kartonska škatla z 1 pretisnim omotom z 10 tabletami.

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:

Dechra Regulatory B.V.

Datum dovoljenja za promet z zdravilom:

10/04/2019

Proizvodna mesta, odgovorna za sproščanje serij:

Lelypharma B.V.
Genera d.d.

Pristojni organ:

Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia

Številka dovoljenja za promet z zdravilom:

DC/V/0663/001

Datum spremembe statusa dovoljenja za promet:

10/04/2019

Referenčna država članica:

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

Številka postopka:

NL/V/0317/001

Zadevne države članice:

Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Croatian Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian Greek English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Latvian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish German Estonian English French Italian Dutch Portuguese Slovak Finnish Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Lithuanian Dutch Portuguese Romanian Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Croatian Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Na voljo samo v Estonian English French Lithuanian Portuguese Swedish Icelandic Norwegian

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

Dokumenti

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Objavljeno na dan: 30/04/2025

Navodilo za uporabo

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Objavljeno na dan: 30/04/2025

Označevanje

slovenščina (PDF)

Objavljeno na dan: 30/04/2025

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