Veterinary Medicines

Aftovaxpur DOE (25) A24 Cruzeiro + A Turkey 14/98

Authorised

Foot-and-mouth disease virus, serotype A, strain A24 Cruzeiro, Inactivated
Foot-and-mouth disease virus, serotype A, strain Turkey 14/98, Inactivated

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Identifikazzjoni tal-prodott

Isem tal-mediċina:

Aftovaxpur DOE (25) A24 Cruzeiro + A Turkey 14/98

Sustanza attiva:

Disponibbli biss fi English
Disponibbli biss fi English

Speċi li fuqhom ser jintuża l-prodott:

Metodu ta’ amministrazzjoni:

Użu għal ġol-muskoli
Użu għal taħt il-ġilda

Dettalji tal-prodott

Sustanza attiva / Qawwa:

Disponibbli biss fi English

Presentation_strength:≥ 6 PD50 Reference:Hse Index:0
Disponibbli biss fi English

Presentation_strength:≥ 6 PD50 Index:11

Forma farmaċewtika:

Emulsjoni għall-injezzjoni

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

Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):

QI02AA04

Status legali tal-provvista:

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Status tal-awtorizzazzjoni:

Valid

Authorised in:

Deskrizzjoni tal-pakkett:

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Disponibbli biss fi English
Disponibbli biss fi English
Disponibbli biss fi English
Disponibbli biss fi English
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Tagħrif addizzjonali

Entitlement type:

Disponibbli biss fi English français italiano latviešu svenska íslenzkan norsk

Bażi ġuridika tal-awtorizzazzjoni tal-prodott:

Disponibbli biss fi English italiano

Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:

Boehringer Ingelheim Vetmedica GmbH

Awtorizzazzjoni għat-tqegħid fis-suq maħruġa:

15/07/2013

Siti ta’ manifattura b’rilaxx tal-lott:

Boehringer Ingelheim Animal Health France

Pajjiż tal-awtorizzazzjoni:

Din l-informazzjoni mhijiex disponibbli għal dan il-prodott.

Awtorità responsabbli:

European Commission

Numru tal-awtorizzazzjoni:

Din l-informazzjoni mhijiex disponibbli għal dan il-prodott.

Data tal-bidla fl-istatus tal-awtorizzazzjoni:

15/07/2013

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

Dokumenti

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Portuguese (PDF)

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

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6/02/2023

English (PDF)

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

Published:

6/02/2023

English (PDF)

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

Published:

17/03/2023

English (PDF)

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