Veterinary Medicines

Mometamax Ultra 8.6 mg/ml + 2.6 mg/ml + 2.1 mg/ml - Ear drops, suspension

Authorised
  • Gentamicin
  • Posaconazole
  • Mometasone furoate
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Product identification

Medicine name:
Mometamax Ultra 8.6 mg/ml + 2.6 mg/ml + 2.1 mg/ml - Ear drops, suspension
Active substance:
  • Gentamicin
  • Posaconazole
  • Mometasone furoate
Target species:
  • Dog
Route of administration:
  • Auricular use

Product details

Active substance and strength:
  • Gentamicin
    6880.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • Posaconazole
    2.08
    milligram(s)
    /
    1.00
    millilitre(s)
  • Mometasone furoate
    1.68
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Ear drops, suspension
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QS02CA91
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
  • Croatia
  • Cyprus
  • Czechia
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Luxembourg
  • Netherlands
  • Poland
  • Romania
  • Slovakia
  • Slovenia
  • Spain
Package description:
  • Packaging:bottle (HDPE), Package_size:1 bottle + 1 adapter (LDPE) + 20 syringes, Content:16 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:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vet Pharma Friesoythe GmbH
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: 28/07/2025
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Bulgarian (PDF)
Published on: 28/07/2025
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Croatian (PDF)
Published on: 28/07/2025
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Czech (PDF)
Published on: 28/07/2025
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Danish (PDF)
Published on: 28/07/2025
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Dutch (PDF)
Published on: 28/07/2025
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Estonian (PDF)
Published on: 28/07/2025
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Finnish (PDF)
Published on: 28/07/2025
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French (PDF)
Published on: 28/07/2025
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German (PDF)
Published on: 28/07/2025
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Greek (PDF)
Published on: 28/07/2025
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Hungarian (PDF)
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Icelandic (PDF)
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Italian (PDF)
Published on: 28/07/2025
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Latvian (PDF)
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Lithuanian (PDF)
Published on: 28/07/2025
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Maltese (PDF)
Published on: 28/07/2025
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Norwegian (PDF)
Published on: 28/07/2025
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Polish (PDF)
Published on: 28/07/2025
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Portuguese (PDF)
Published on: 28/07/2025
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Romanian (PDF)
Published on: 28/07/2025
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Slovak (PDF)
Published on: 28/07/2025
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Slovenian (PDF)
Published on: 28/07/2025
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Spanish (PDF)
Published on: 28/07/2025
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Swedish (PDF)
Published on: 28/07/2025
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ema-puar-mometamax-ultra-v-004987-par-en.pdf

English (PDF)
Published on: 15/05/2023
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