Veterinary Medicines

Cronyxin 50 mg/g Oral paste for horses

Authorised
  • Flunixin meglumine
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Product identification

Medicine name:
Cronyxin 50 mg/g Oral paste for horses
Cronyxin Vet. 50 mg/g oral pasta
Active substance:
  • Flunixin meglumine
Target species:
  • Horse
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Flunixin meglumine
    83.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Oral paste
Withdrawal period by route of administration:
  • Oral use
    • Horse
      • Meat and offal
        15
        day
      • Milk
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AG90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Denmark
Package description:
  • (ID5) 396 gram(s): unspecified outer container with 12 Applicator (high-density polyethylene) each with 33 gram(s)
  • (ID4) 198 gram(s): unspecified outer container with 6 Applicator (high-density polyethylene) each with 33 gram(s)
  • (ID3) 99 gram(s): unspecified outer container with 3 Applicator (high-density polyethylene) each with 33 gram(s)
  • (ID2) 66 gram(s): unspecified outer container with 2 Applicator (high-density polyethylene) each with 33 gram(s)
  • (ID1) 33 gram(s): unspecified outer container with 1 Applicator (high-density polyethylene) with 33 gram(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:
  • Bimeda Animal Health Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bimeda Animal Health Limited
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 60049
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0178/001
Concerned member states:
  • Austria
  • Belgium
  • Denmark
  • Estonia
  • Finland
  • France
  • Ireland
  • Italy
  • Netherlands
  • Poland
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Danish (, ORAL PASTA 50 MG-G)
Published on: 29/06/2023
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Combined File of all Documents

English (PDF)
Published on: 27/01/2026
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2402471-paren-20230821.pdf

English (PDF)
Published on: 27/01/2026
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