Veterinary Medicines

DIVENCE Tetra (--) Lyophilisate and solvent for emulsion for injection

Authorised
  • Bovine respiratory syncytial virus, strain Lym-56, Live
  • Bovine parainfluenza virus 3, strain SF-4, Inactivated
  • Bovine viral diarrhoea virus 1, protein E2 (recombinant)
  • Bovine viral diarrhoea virus 2, protein E2 (recombinant)
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Product identification

Medicine name:
DIVENCE Tetra (--) Lyophilisate and solvent for emulsion for injection
Active substance:
  • Bovine respiratory syncytial virus, strain Lym-56, Live
  • Bovine parainfluenza virus 3, strain SF-4, Inactivated
  • Bovine viral diarrhoea virus 1, protein E2 (recombinant)
  • Bovine viral diarrhoea virus 2, protein E2 (recombinant)
Target species:
  • Cattle
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Bovine respiratory syncytial virus, strain Lym-56, Live
    Presentation_strength:10⁵·² - 10⁶·⁵ CCID50 Comments:lyophilisate Index:0
  • Bovine parainfluenza virus 3, strain SF-4, Inactivated
    Presentation_strength:≥ 206.2 EU Comments:lyophilisate Index:1
  • Bovine viral diarrhoea virus 1, protein E2 (recombinant)
    Presentation_strength:≥ 31.6 EU Comments:lyophilisate Index:2
  • Bovine viral diarrhoea virus 2, protein E2 (recombinant)
    Presentation_strength:≥ 21.0 EU Comments:lyophilisate Index:3
Pharmaceutical form:
  • Lyophilisate and solvent for emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AH
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:Lyophilisate: vial (glass); Solvent: vial (PET), Package_size:Lyophilisate: 1 vial + Solvent: 1 vial, Content:Lyophilisate: 20 doses; Solvent: 40 ml
  • Packaging:Lyophilisate: vial (glass); Solvent: vial (PET), Package_size:Lyophilisate: 1 vial + Solvent: 1 vial, Content:Lyophilisate: 10 doses; Solvent: 20 ml
  • Packaging:Lyophilisate: vial (glass); Solvent: vial (PET), Package_size:Lyophilisate: 1 vial + Solvent: 1 vial, Content:Lyophilisate: 5 doses; Solvent: 10 ml

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - new active substance (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • LABORATORIOS HIPRA,S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratorios Hipra S.A.
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: 8/12/2025
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Bulgarian (PDF)
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Croatian (PDF)
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Czech (PDF)
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Danish (PDF)
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Dutch (PDF)
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Estonian (PDF)
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Finnish (PDF)
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French (PDF)
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German (PDF)
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Greek (PDF)
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Hungarian (PDF)
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Icelandic (PDF)
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Italian (PDF)
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Latvian (PDF)
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Lithuanian (PDF)
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Maltese (PDF)
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Norwegian (PDF)
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Polish (PDF)
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Portuguese (PDF)
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Romanian (PDF)
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Slovak (PDF)
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Slovenian (PDF)
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Spanish (PDF)
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Swedish (PDF)
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ema-puar-v6222-divencetetra-en.pdf

English (PDF)
Published on: 28/08/2024
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