Veterinary Medicines

Animeloxan, 20 mg/ml, solution for injection for cattle, pigs and horses

Authorised
  • Meloxicam
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Product identification

Medicine name:
Animeloxan, 20 mg/ml, solution for injection for cattle, pigs and horses
Animeloxan, 20 mg/ml, solution for injection for cattle, pigs and horses
Active substance:
  • Meloxicam
Target species:
  • Cattle
  • Horse
  • Pig
Route of administration:
  • Intravenous use
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Meloxicam
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Milk
        5
        day
      • Meat and offal
        15
        day
    • Horse
      • Milk
        no withdrawal period
      • Meat and offal
        5
        day
  • Subcutaneous use
    • Cattle
      • Milk
        5
        day
      • Meat and offal
        15
        day
  • Intramuscular use
    • Pig
      • Meat and offal
        8
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AC06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • (ID4): 1 unspecified outer container with 12 Vial (Glass) with 100 millilitre(s) (1200 millilitre(s))
  • (ID3): 1 unspecified outer container with 12 Vial (Glass) with 50 millilitre(s) (600 millilitre(s))
  • (ID2): 1 unspecified outer container with 1 Vial (-) with 100 millilitre(s) (100 millilitre(s))
  • (ID1): 1 unspecified outer container with 1 Vial (-) with 50 millilitre(s) (50 millilitre(s))

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
  • Industrial Veterinaria S.A.
  • aniMedica Herstellungs GmbH
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10826/025/001
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0311/002
Concerned member states:
  • Austria
  • Bulgaria
  • Cyprus
  • Czechia
  • Estonia
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 14/02/2022
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Combined File of all Documents

English (PDF)
Published on: 5/06/2023
Download
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