Intercam 0.5 mg/ml oral suspension for cats
Intercam 0.5 mg/ml oral suspension for cats
Authorised
- Meloxicam
Product identification
Medicine name:
Intercam 0.5 mg/ml oral suspension for cats
ARTHROKAN CLEMENT THEKAN 0,5 MG/ML SUSPENSION BUVABLE POUR CHATS
Active substance:
- Meloxicam
Target species:
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Meloxicam0.50/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AC06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
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:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/2601522 4/2023
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0882/001
Concerned member states:
-
France
-
Portugal
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 6/07/2025
French (PDF)
Published on: 3/06/2024
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 15/10/2025
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