Veterinary Medicines Information website

Strangvac (--) - Suspension for injection

Authorised
  • Streptococcus equi subsp. equi, recombinant protein CCE
  • Streptococcus equi subsp. equi, recombinant protein Eq85
  • Streptococcus equi subsp. equi, recombinant protein IdeE
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Product identification

Medicine name:
Strangvac (--) - Suspension for injection
Active substance:
  • Streptococcus equi subsp. equi, recombinant protein CCE
  • Streptococcus equi subsp. equi, recombinant protein Eq85
  • Streptococcus equi subsp. equi, recombinant protein IdeE
Target species:
  • Horse
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Streptococcus equi subsp. equi, recombinant protein CCE
    Presentation_strength:≥111.8 μg Reference:Hse Index:0
  • Streptococcus equi subsp. equi, recombinant protein Eq85
    Presentation_strength:≥44.6 μg Reference:Hse Index:1
  • Streptococcus equi subsp. equi, recombinant protein IdeE
    Presentation_strength:≥34.6 μg Reference:Hse Index:2
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Horse
      • Not applicable
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI05AB01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • 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)
Package description:
  • Packaging:Vial (glass), Package_size:8 vials, Content:2 ml

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - New active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervacc AB
Marketing authorisation date:
Manufacturing sites for batch release:
  • 3 P Biopharmaceuticals S.L.
Responsible authority:
  • European Commission
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Combined File of all Documents

English (PDF)
Published on: 6/10/2026
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Czech (PDF)
Published on: 6/10/2026
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Danish (PDF)
Published on: 6/10/2026
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German (PDF)
Published on: 6/10/2026
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Greek (PDF)
Published on: 6/10/2026
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Bulgarian (PDF)
Published on: 6/10/2026
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Spanish (PDF)
Published on: 6/10/2026
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Estonian (PDF)
Published on: 6/10/2026
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Finnish (PDF)
Published on: 6/10/2026
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French (PDF)
Published on: 6/10/2026
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Croatian (PDF)
Published on: 6/10/2026
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Hungarian (PDF)
Published on: 6/10/2026
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Icelandic (PDF)
Published on: 6/10/2026
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Italian (PDF)
Published on: 6/10/2026
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Lithuanian (PDF)
Published on: 6/10/2026
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Latvian (PDF)
Published on: 6/10/2026
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Maltese (PDF)
Published on: 6/10/2026
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Dutch (PDF)
Published on: 6/10/2026
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Norwegian (PDF)
Published on: 6/10/2026
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Polish (PDF)
Published on: 6/10/2026
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Portuguese (PDF)
Published on: 6/10/2026
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Romanian (PDF)
Published on: 6/10/2026
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Slovak (PDF)
Published on: 6/10/2026
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Slovenian (PDF)
Published on: 6/10/2026
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Swedish (PDF)
Published on: 6/10/2026
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ema-puar-strangvac-epar-public-assessment-report-en.pdf

English (PDF)
Published on: 14/03/2026
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