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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Identifikácia lieku

Názov lieku:

Aftovaxpur DOE (60) O1 BFS + SAT2 Saudi Arabia

Účinná látka:

Dostupné len v English
Dostupné len v English

Cesta podania:

Intramuskulárne použitie
Subkutánne použitie

Podrobnosti o lieku

Účinná látka a sila:

Dostupné len v English

Presentation_strength:≥ 6 PD50 Reference:Hse Index:0
Dostupné len v English

Presentation_strength:≥ 6 PD50 Index:11

Lieková forma:

Injekčná emulzia

Withdrawal period by route of administration:

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

Anatomicko-terapeuticko-chemický veterinárny kód (ATCvet):

QI02AA04

Právny stav dodávky:

Dostupné len v čeština eesti English français italiano latviešu português slovenščina svenska norsk

Stav registrácie:

Valid

Authorised in:

Opis balenia:

Dostupné len v English
Dostupné len v English
Dostupné len v English
Dostupné len v English
Dostupné len v English
Dostupné len v English
Dostupné len v English
Dostupné len v English
Dostupné len v English
Dostupné len v English

Ďalšie informácie

Typ postupu registrácie:

Dostupné len v English français italiano latviešu svenska íslenzkan norsk

Právny základ pre registráciu produktu:

Dostupné len v English italiano

Držiteľ rozhodnutia o registrácii:

Boehringer Ingelheim Vetmedica GmbH

Vydané rozhodnutie o registrácii:

15/07/2013

Miesta výroby na uvoľnenie šarže:

Boehringer Ingelheim Animal Health France

Schvaľujúca krajina:

Požadované informácie o tomto lieku nie sú k dispozícii.

Zodpovedný orgán:

European Commission

Číslo registrácie:

Požadované informácie o tomto lieku nie sú k dispozícii.

Dátum zmeny stavu registrácie:

7/04/2014

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

Dokumenty

Combined File of all Documents

Published:

4/11/2022

Bulgarian (PDF)

Combined File of all Documents

Published:

4/11/2022

Czech (PDF)

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Published:

4/11/2022

Danish (PDF)

Combined File of all Documents

Published:

4/11/2022

German (PDF)

Combined File of all Documents

Published:

4/11/2022

Greek (PDF)

Combined File of all Documents

Published:

4/11/2022

English (PDF)

Combined File of all Documents

Published:

4/11/2022

Spanish (PDF)

Combined File of all Documents

Published:

4/11/2022

Estonian (PDF)

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Published:

4/11/2022

Finnish (PDF)

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Published:

4/11/2022

French (PDF)

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4/11/2022

Croatian (PDF)

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4/11/2022

Hungarian (PDF)

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4/11/2022

Icelandic (PDF)

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4/11/2022

Italian (PDF)

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4/11/2022

Lithuanian (PDF)

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4/11/2022

Latvian (PDF)

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4/11/2022

Maltese (PDF)

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4/11/2022

Dutch (PDF)

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4/11/2022

Polish (PDF)

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4/11/2022

Romanian (PDF)

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Published:

4/11/2022

slovenčina (PDF)

Combined File of all Documents

Published:

4/11/2022

Slovenian (PDF)

Combined File of all Documents

Published:

4/11/2022

Swedish (PDF)

Combined File of all Documents

Published:

4/11/2022

Norwegian (PDF)

Combined File of all Documents

Published:

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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