Zulvac 1+8 Bovis

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Authorised

This medicine is authorised for use in the European Union

inactivated bluetongue virus, serotypes 1 and 8
MedicineVeterinaryAuthorised

Czech is available via eTranslation, the European Commission's machine translation service.

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  • Application under evaluation
  • CVMP opinion
  • European Commission decision

Overview

Up-to-date information on this veterinary medicinal product is available on the Veterinary Medicines Information website

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Product information

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български (BG) (93.36 KB - PDF)

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español (ES) (81.97 KB - PDF)

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čeština (CS) (93.99 KB - PDF)

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dansk (DA) (83.34 KB - PDF)

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Deutsch (DE) (82.76 KB - PDF)

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eesti (ET) (82.18 KB - PDF)

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ελληνικά (EL) (93.76 KB - PDF)

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français (FR) (82.44 KB - PDF)

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Gaeilge (GA) (83.57 KB - PDF)

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hrvatski (HR) (92.27 KB - PDF)

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italiano (IT) (82.29 KB - PDF)

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latviešu (LV) (94.29 KB - PDF)

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lietuvių (LT) (94.03 KB - PDF)

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polski (PL) (95.62 KB - PDF)

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português (PT) (83.01 KB - PDF)

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română (RO) (94.17 KB - PDF)

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slovenčina (SK) (94.08 KB - PDF)

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slovenščina (SL) (82.27 KB - PDF)

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suomi (FI) (81.54 KB - PDF)

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svenska (SV) (82.05 KB - PDF)

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Íslenska (IS) (83.29 KB - PDF)

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norsk (NO) (82 KB - PDF)

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Product details

Name of medicine
Zulvac 1+8 Bovis
Active substance
  • inactivated bluetongue virus, serotype 1, strain BTV-1/ALG2006/01 E1 RP
  • inactivated bluetongue virus, serotype 8, strain btv-8/bel2006/02
International non-proprietary name (INN) or common name
inactivated bluetongue virus, serotypes 1 and 8

Pharmacotherapeutic group

  • Immunologicals
  • Immunologicals for Bovidae
  • Cattle
  • Inactivated viral vaccines
  • bluetongue virus

Authorisation details

EMA product number
EMEA/V/C/002473

Accelerated assessment

This medicine had an accelerated assessment. This means that it is a medicine of major interest for public health, so its timeframe for review was 150 evaluation days rather than 210. For more information, see Accelerated assessment.

Assessment history

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