Veterinary Medicines

Metaxx 1.5 mg/ml oral suspension for dogs

Authorised
  • Meloxicam
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Product identification

Medicine name:
Metaxx 1.5 mg/ml oral suspension for dogs
Mexxam Vet 1,5 mg/ml Suspension zum Eingeben für Hunde
Active substance:
  • Meloxicam
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Meloxicam
    1.50
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AC06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
Package description:
  • 5 ml (in a 10 ml sized bottle). Cardboard box with one HDPE bottle with an LDPE syringe adapter and closed with a polypropylene screw cap. Polypropylene measuring syringe of 3 mL.
  • 10 ml. Cardboard box with one HDPE bottle with an LDPE syringe adapter and closed with a polypropylene screw cap. Polypropylene measuring syringe of 3 mL.
  • 25 ml. Cardboard box with one HDPE bottle with an LDPE syringe adapter and closed with a polypropylene screw cap. Polypropylene measuring syringe of 3 mL.
  • 50 ml. Cardboard box with one HDPE bottle with an LDPE syringe adapter and closed with a polypropylene screw cap. Polypropylene measuring syringe of 3 mL.
  • 125 ml. Cardboard box with one HDPE bottle with an LDPE syringe adapter and closed with a polypropylene screw cap. Polypropylene measuring syringe of 3 mL.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Alfasan Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Alfasan Nederland B.V.
  • Produlab Pharma B.V.
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 842208
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0399/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)
Generic of:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 20/06/2024
Updated on: 24/02/2025
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 20/06/2024
Updated on: 24/02/2025
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 20/06/2024
Updated on: 24/02/2025
Download
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