Veterinary Medicine Information website

Zeleris 400 mg/ml florfenicol + 5 mg/ml meloxicam - Solution for injection

Authorised
  • Florfenicol
  • Meloxicam
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Product identification

Medicine name:
Zeleris 400 mg/ml florfenicol + 5 mg/ml meloxicam - Solution for injection
Active substance:
  • Florfenicol
  • Meloxicam
Target species:
  • Cattle
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Florfenicol
    400.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Meloxicam
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        56
        day
      • Milk
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01BA99
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)
Available in:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
Package description:
  • Packaging:Vial (PP/EVOH/PP), Package_size:1 vial, Content:250 ml
  • Packaging:Vial (PP/EVOH/PP), Package_size:1 vial, Content:100 ml
  • Packaging:Vial (PP/EVOH/PP), Package_size:1 vial, Content:50 ml

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Fixed combination application (Article 13b of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Sante Animale
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: 16/09/2025
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Czech (PDF)
Published on: 16/09/2025
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German (PDF)
Published on: 16/09/2025
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Danish (PDF)
Published on: 16/09/2025
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Greek (PDF)
Published on: 16/09/2025
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Bulgarian (PDF)
Published on: 16/09/2025
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Estonian (PDF)
Published on: 16/09/2025
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Spanish (PDF)
Published on: 16/09/2025
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Lithuanian (PDF)
Published on: 16/09/2025
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Italian (PDF)
Published on: 16/09/2025
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Dutch (PDF)
Published on: 16/09/2025
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Maltese (PDF)
Published on: 16/09/2025
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Finnish (PDF)
Published on: 16/09/2025
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French (PDF)
Published on: 16/09/2025
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Icelandic (PDF)
Published on: 16/09/2025
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Croatian (PDF)
Published on: 16/09/2025
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Latvian (PDF)
Published on: 16/09/2025
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Norwegian (PDF)
Published on: 16/09/2025
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Swedish (PDF)
Published on: 16/09/2025
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Polish (PDF)
Published on: 16/09/2025
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Romanian (PDF)
Published on: 16/09/2025
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Slovenian (PDF)
Published on: 16/09/2025
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Portuguese (PDF)
Published on: 16/09/2025
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Slovak (PDF)
Published on: 16/09/2025
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Hungarian (PDF)
Published on: 16/09/2025
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ema-puar-v4099-zeleris-vra-0005-g-en.pdf

English (PDF)
Published on: 13/12/2023
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ema-puar-zeleris-v-4099-par-en.pdf

English (PDF)
Published on: 16/03/2023
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