Veterinary Medicines

Aftovaxpur DOE (60) O1 BFS + SAT2 Saudi Arabia

Authorised

Foot-and-mouth disease virus, serotype O, strain O1 BFS, Inactivated
Foot-and-mouth disease virus, serotype SAT2, strain Saudi Arabia, Inactivated

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Identifikacija zdravila

Ime zdravila:

Aftovaxpur DOE (60) O1 BFS + SAT2 Saudi Arabia

Učinkovina:

Na voljo samo v English
Na voljo samo v English

Ciljne živalske vrste:

Pot uporabe:

intramuskularna uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

Presentation_strength:≥ 6 PD50 Reference:Hse Index:0
Na voljo samo v English

Presentation_strength:≥ 6 PD50 Index:11

Farmacevtska oblika:

Emulzija za injiciranje

Withdrawal period by route of administration:

Intramuscular use
- govedo
  - Not applicable
    
    0
    
    day
    
    Zero days
- Sheep
  - Not applicable
    
    0
    
    day
    
    Zero days
- Pig
  - Not applicable
    
    0
    
    day
    
    Zero days
Subcutaneous use
- govedo
  - Not applicable
    
    0
    
    day
    
    Zero days
- Sheep
  - Not applicable
    
    0
    
    day
    
    Zero days
- Pig
  - Not applicable
    
    0
    
    day
    
    Zero days

Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):

QI02AA04

Pravni status za dobavo / izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja:

Valid

Authorised in:

Opis ovojnine:

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

Dodatne informacije

Vrsta postopka za pridobitev dovoljenja:

Na voljo samo v English français italiano latviešu svenska íslenzkan norsk

Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English italiano

Imetnik dovoljenja za promet z zdravilom:

Boehringer Ingelheim Vetmedica GmbH

Izdano dovoljenje za promet z zdravilom:

15/07/2013

Proizvodna mesta, odgovorna za sproščanje serij:

Boehringer Ingelheim Animal Health France

Država izdaje dovoljenja:

Ta podatek za to zdravilo ni na voljo.

Pristojni organ:

European Commission

Številka dovoljenja :

Ta podatek za to zdravilo ni na voljo.

Datum spremembe statusa dovoljenja:

7/04/2014

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Dokumenti

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Published:

4/11/2022

Bulgarian (PDF)

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4/11/2022

Czech (PDF)

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Danish (PDF)

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4/11/2022

German (PDF)

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4/11/2022

Greek (PDF)

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4/11/2022

English (PDF)

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4/11/2022

Spanish (PDF)

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4/11/2022

Estonian (PDF)

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Finnish (PDF)

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French (PDF)

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Croatian (PDF)

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Hungarian (PDF)

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Italian (PDF)

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Lithuanian (PDF)

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Latvian (PDF)

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Maltese (PDF)

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Dutch (PDF)

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Polish (PDF)

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Romanian (PDF)

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Slovak (PDF)

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4/11/2022

slovenščina (PDF)

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4/11/2022

Swedish (PDF)

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4/11/2022

Norwegian (PDF)

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4/11/2022

Portuguese (PDF)

ema-puar-aftovaxpur-v-2292-par-en.pdf

Published:

6/02/2023

English (PDF)

ema-puar-aftovaxpur-v-2292-var-ii-0009-en.pdf

Published:

6/02/2023

English (PDF)

ema-puar-aftovaxpur-v-2292-var-ii-0001-en.pdf

Published:

6/02/2023

English (PDF)

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