Zeleris 400 mg/ml florfenicol + 5 mg/ml meloxicam - Solution for injection
Zeleris 400 mg/ml florfenicol + 5 mg/ml meloxicam - Solution for injection
Authorised
- Florfenicol
- Meloxicam
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:
-
Florfenicol400.00/milligram(s)1.00millilitre(s)
-
Meloxicam5.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal56day56 days
-
Milkno withdrawal period999 days - Not authorised for use in animals producing milk for human consumption
-
-
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 Santé 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:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 13/12/2023
Bulgarian (PDF)
Published on: 13/12/2023
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)
Published on: 13/12/2023
Romanian (PDF)
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Slovak (PDF)
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Slovenian (PDF)
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Spanish (PDF)
Published on: 13/12/2023
Swedish (PDF)
Published on: 13/12/2023
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