Veterinary Medicines

Animeloxan 1.5 mg/ml oral suspension for dogs

Authorised
  • Meloxicam
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Product identification

Medicine name:
Animeloxan 1.5 mg/ml oral suspension for dogs
Animeloxan 1,5 mg/ml suspensie voor oraal gebruik bij honden
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
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AC06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • (ID3) 100 millilitre(s): Box (Cardboard) with 1 Bottle (Polyethylen hoher Dichte) with 100 millilitre(s), closed with Lid and Verschluss mit Tropfer (Polyethylen, Polyethylen)
  • (ID1) 10 millilitre(s): Box (Cardboard) with 1 Bottle (Polyethylen hoher Dichte) with 10 millilitre(s), closed with Lid and Verschluss mit Tropfer (Polyethylen, Polyethylen)
  • (ID6) 125 millilitre(s): Box (Cardboard) with 1 Bottle (Polyethylen hoher Dichte) with 125 millilitre(s), closed with Verschluss mit Tropfer and Lid (Polyethylen, Polyethylen)
  • (ID4) 25 millilitre(s): Box (Cardboard) with 1 Bottle (Polyethylen hoher Dichte) with 25 millilitre(s), closed with Verschluss mit Tropfer and Lid (Polyethylen, Polyethylen)
  • (ID5) 50 millilitre(s): Box (Cardboard) with 1 Bottle (Polyethylen hoher Dichte) with 50 millilitre(s), closed with Lid and Verschluss mit Tropfer (Polyethylen, Polyethylen)

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:
  • aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • aniMedica GmbH
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 100187
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0310/001
Concerned member states:
  • Austria
  • Denmark
  • Hungary
  • Italy
  • Netherlands
  • Poland
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 7/12/2022
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Combined File of all Documents

English (PDF)
Published on: 1/09/2023
Updated on: 4/09/2023
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Dutch (PDF)
Published on: 30/01/2023
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