HorStem 15 x 10⁶ cells/ml - Suspension for injection

Ima dovoljenje za promet

Equine allogeneic umbilical cord-derived mesenchymal stem cells

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Informacije o zdravilu

Ime zdravila:

HorStem 15 x 10⁶ cells/ml - Suspension for injection

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

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Pot uporabe:

Intraartikularna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

Presentation_strength:15,000,000 cells Comments:range from 12,000,000 to 18,000,000 cells/ml Index:0

Farmacevtska oblika:

Suspenzija za injiciranje

Karenca glede na pot uporabe:

Intraartikularna uporaba
- Horse
  - Not applicable
    
    0
    
    day
    
    Zero days

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

QM09AX

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:

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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

Na voljo v:

Austria
Belgium
Denmark
France
Germany
Ireland
Netherlands
Norway
Poland
Spain
Sweden

Opis ovojnine zdravila:

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:

EquiCord S.L.

Datum dovoljenja za promet z zdravilom:

19/06/2019

Proizvodna mesta, odgovorna za sproščanje serij:

EquiCord S.L.

Pristojni organ:

European Commission

Številka dovoljenja za promet z zdravilom:

Ta podatek za to zdravilo ni na voljo.

Datum spremembe statusa dovoljenja za promet:

19/06/2019

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

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HorStem 15 x 10⁶ cells/ml - Suspension for injection

Informacije o zdravilu

Podatki o zdravilu

Dodatne informacije

Dokumenti

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