Veterinary Medicines

Metaxx 5 mg/ml solution for injection for cattle, pigs, dogs and cats

Authorised
  • Meloxicam
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Product identification

Medicine name:
Metaxx 5 mg/ml solution for injection for cattle, pigs, dogs and cats
Metaxx 5 mg/ml ενέσιμο διάλυμα για βοοειδή, χοίρους, σκύλους και γάτες
Active substance:
  • Meloxicam
Target species:
  • Dog
  • Cat
  • Cattle
  • Pig
Route of administration:
  • Subcutaneous use
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Meloxicam
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Concentrate for solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Dog
      • Not applicable
        no withdrawal period
    • Cat
      • Not applicable
        no withdrawal period
    • Cattle
      • Meat and offal
        no withdrawal period
  • Intramuscular use
    • Pig
      • Meat and offal
        no withdrawal period
  • Intravenous use
    • Cattle
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AC06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Cyprus
Package description:
  • Colourless glass (type I) injection vial , closed with a rubber stopper and sealed with an aluminium cap. Cardboard box of 1 vial of 250 ml
  • Colourless glass (type I) injection vial , closed with a rubber stopper and sealed with an aluminium cap. Cardboard box of 1 vial of 100 ml
  • Colourless glass (type I) injection vial , closed with a rubber stopper and sealed with an aluminium cap. Cardboard box of 1 vial of 50 ml
  • Colourless glass (type I) injection vial , closed with a rubber stopper and sealed with an aluminium cap

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic (abridged application) - art 13(1)
Marketing authorisation holder:
  • Alfasan Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Produlab Pharma B.V.
  • Alfasan Nederland B.V.
Responsible authority:
  • Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
  • CY00884V
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0375/001
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)

Documents

Combined File of all Documents

English (PDF)
Published on: 17/05/2023
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Greek (PDF)
Published on: 18/03/2025
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