Veterinary Medicines

Intercam 0.5 mg/ml oral suspension for cats

Authorised
  • Meloxicam
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Product identification

Medicine name:
Intercam 0.5 mg/ml oral suspension for cats
Meloxyl 0,5 mg/ml suspensão oral para gatos
Active substance:
  • Meloxicam
Target species:
  • Cat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Meloxicam
    0.50
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Oral suspension
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AC06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Portugal
Package description:
  • Polypropylene bottle containing 5 ml with a tamper proof child resistant closures.Each bottle is packed in a cardboard box with a 1 ml measuring syringe (barrel in polypropylene and plunger/piston in high density polyethylene).
  • Polypropylene bottle containing 3 ml with a tamper proof child resistant closures.Each bottle is packed in a cardboard box with a 1 ml measuring syringe (barrel in polypropylene and plunger/piston in high density polyethylene).
  • White high density polyethylene bottle containing 10 ml with a tamper proof child resistant closure.Each bottle is packed in a cardboard box with a 1 ml measuring syringe (barrel in polypropylene and plunger/piston in high density polyethylene).
  • White high density polyethylene bottle containing 15 ml with a tamper proof child resistant closure.Each bottle is packed in a cardboard box with a 1 ml measuring syringe (barrel in polypropylene and plunger/piston in high density polyethylene).

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:
  • C&H Generics Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • 1606/01/23RFVPT
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0882/001
Concerned member states:
  • France
  • Portugal
  • Spain

Documents

Combined File of all Documents

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Portuguese (PDF)
Published on: 17/10/2024
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Summary of Product Characteristics

English (PDF)
Published on: 6/07/2025
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