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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

Identifikazzjoni tal-prodott

Isem tal-mediċina:
Aftovaxpur DOE (25) A24 Cruzeiro + A Turkey 14/98
Sustanza attiva:
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
    • Sheep
      • Not applicable
        0
        day
    • Pig
      • Not applicable
        0
        day
  • Subcutaneous use
    • Cattle
      • Not applicable
        0
        day
    • Sheep
      • Not applicable
        0
        day
    • Pig
      • Not applicable
        0
        day
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
  • QI02AA04
Status tal-awtorizzazzjoni:
  • Valid
Authorised in:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)
Deskrizzjoni tal-pakkett:

Tagħrif addizzjonali

Entitlement type:
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
  • Boehringer Ingelheim Vetmedica GmbH
Awtorizzazzjoni għat-tqegħid fis-suq maħruġa:
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:

Dokumenti

Combined File of all Documents

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Bulgarian (PDF)
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Czech (PDF)
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Combined File of all Documents

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Danish (PDF)
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Combined File of all Documents

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German (PDF)
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Combined File of all Documents

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Greek (PDF)
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Combined File of all Documents

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English (PDF)
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Combined File of all Documents

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Spanish (PDF)
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Combined File of all Documents

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Estonian (PDF)
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Combined File of all Documents

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Finnish (PDF)
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Combined File of all Documents

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French (PDF)
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Combined File of all Documents

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Croatian (PDF)
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Combined File of all Documents

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Hungarian (PDF)
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Combined File of all Documents

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Icelandic (PDF)
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Combined File of all Documents

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Italian (PDF)
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Combined File of all Documents

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Lithuanian (PDF)
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Combined File of all Documents

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Latvian (PDF)
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Combined File of all Documents

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Malti (PDF)
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Combined File of all Documents

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Dutch (PDF)
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Combined File of all Documents

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Polish (PDF)
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Combined File of all Documents

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Romanian (PDF)
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Combined File of all Documents

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Slovak (PDF)
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Combined File of all Documents

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Slovenian (PDF)
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Combined File of all Documents

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Swedish (PDF)
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Combined File of all Documents

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Norwegian (PDF)
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Combined File of all Documents

Published:
Portuguese (PDF)
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ema-puar-aftovaxpur-v-2292-par-en.pdf

Published:
English (PDF)
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ema-puar-aftovaxpur-v-2292-var-ii-0001-en.pdf

Published:
English (PDF)
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ema-puar-aftovaxpur-v-2292-var-ii-0009-en.pdf

Published:
English (PDF)
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