Veterinary Medicines

Melosolute 5 mg/ml Solution for injection for cattle, pigs, dogs and cats

Authorised
  • Meloxicam
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Product identification

Medicine name:
Melosolute 5 mg/ml Solution for injection for cattle, pigs, dogs and cats
Melosolute 5 mg/ml Injektionslösung für Rinder, Schweine, Hunde und Katzen
Active substance:
  • Meloxicam
Target species:
  • Cattle
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Meloxicam
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        15
        day
    • Pig
      • Meat and offal
        5
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        15
        day
    • Pig
      • Meat and offal
        5
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        15
        day
    • Pig
      • Meat and offal
        5
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AC06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:
  • 20 ml injection vial colourless glass (type I), closed with a bromobutyl rubber stopper and sealed with an aluminium cap in a cardboard box
  • 100 ml injection vial colourless glass (type I), closed with a bromobutyl rubber stopper and sealed with an aluminium cap in a cardboard box
  • 10 ml injection vial colourless glass (type I), closed with a bromobutyl rubber stopper and sealed with an aluminium cap in a cardboard box

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • CP-Pharma Handelsgesellschaft mbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • CP-Pharma Handelsgesellschaft mbH
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 401591.00.00
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0164/001
Concerned member states:
  • France
  • Germany
  • Hungary

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (RTF)
Published on: 13/01/2025
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Combined File of all Documents

English (PDF)
Published on: 26/11/2025
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Final PuAR Melosolute NL_V_0164_001-002_DC.docx.pdf

English (PDF)
Published on: 26/11/2025
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