Mhyosphere PCV ID (--) - Emulsion for injection

Ima dovoljenje za promet

Mycoplasma hyopneumoniae, strain Nexhyon, expressing capsid protein of porcine circovirus type 2A, Inactivated

Prenes kot PDF

Informacije o zdravilu

Ime zdravila:

Mhyosphere PCV ID (--) - Emulsion for injection

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

Pot uporabe:

Intradermalna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

Presentation_strength:RP* ≥1.3 Reference:HSE Index:0

Farmacevtska oblika:

Emulzija za injiciranje

Karenca glede na pot uporabe:

Intradermalna uporaba
- Pig
  - Not applicable
    
    0
    
    day
    
    Zero days

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

QI09AL08

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 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 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 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

Opis ovojnine zdravila:

Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English

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 Lithuanian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Laboratorios Hipra, S.A.

Datum dovoljenja za promet z zdravilom:

18/09/2020

Proizvodna mesta, odgovorna za sproščanje serij:

Laboratorios Hipra S.A.

Pristojni organ:

European Commission

Številka dovoljenja za promet z zdravilom:

Ta podatek za to zdravilo ni na voljo.

Datum spremembe statusa dovoljenja za promet:

18/09/2020

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

Dokumenti

Combined File of all Documents

slovenščina (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Drugi jeziki (24)

English (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Finnish (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

French (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Croatian (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Hungarian (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Icelandic (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Bulgarian (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Czech (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Danish (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

German (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Greek (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Estonian (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Spanish (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Italian (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Swedish (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Dutch (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Norwegian (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Slovak (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Lithuanian (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Maltese (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Romanian (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Portuguese (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Polish (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

Latvian (PDF)

Objavljeno na dan: 27/01/2026

Prenesi

ema-puar-mhyosphere-pcv-id-v-5272-par-en.pdf

English (PDF)

Objavljeno na dan: 15/03/2023

Prenesi

Mhyosphere PCV ID (--) - Emulsion for injection

Informacije o zdravilu

Podatki o zdravilu

Dodatne informacije

Dokumenti

Informacije o zdravilu

Javno poročilo o oceni zdravila