Veterinary Medicines

RHEUMOXIDYL 20 MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS AND HORSES

Authorised
This information is not available for this product.
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Product identification

Medicine name:
RHEUMOXIDYL 20 MG/ML SOLUTION FOR INJECTION FOR CATTLE, PIGS AND HORSES
Rheumoxidyl 20 mg/ml Oplossing voor injectie
Rheumoxidyl 20 mg/ml Solution injectable
Rheumoxidyl 20 mg/ml Injektionslösung
Active substance:
This information is not available for this product.
Target species:
  • Pig
  • Cattle
  • Horse
Route of administration:
  • Intramuscular use
  • Subcutaneous use
  • Intravenous use

Product details

Active substance and strength:
This information is not available for this product.
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        5
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        15
        day
      • Milk
        120
        hour
  • Intravenous use
    • Cattle
      • Meat and offal
        15
        day
      • Milk
        120
        hour
    • Horse
      • Milk
        no withdrawal period
      • Meat and offal
        5
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AC06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • Cardboard box with 1 colourless glass injection vial containing 20 ml
  • Cardboard box with 1 colourless glass injection vial containing 50 ml
  • Cardboard box with 1 colourless glass injection vial containing 100 ml
  • Cardboard box with 1 colourless glass injection vial containing 250 ml.

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:
  • Labiana Life Sciences S.A.
  • Chanelle Pharmaceuticals Manufacturing Limited
  • Eurovet Animal Health B.V.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V661413
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0448/001
Concerned member states:
  • Belgium
  • Germany
  • Netherlands

Documents

Combined File of all Documents

English (PDF)
Published on: 13/06/2023
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Summary of Product Characteristics

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Dutch (PDF)
Published on: 13/06/2023
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French (PDF)
Published on: 13/06/2023
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German (PDF)
Published on: 13/06/2023
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Labelling

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Dutch (PDF)
Published on: 13/06/2023
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French (PDF)
Published on: 13/06/2023
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German (PDF)
Published on: 13/06/2023
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 13/06/2023
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French (PDF)
Published on: 13/06/2023
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German (PDF)
Published on: 13/06/2023
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