Veterinary Medicines

CHORULON 5000 LYOPHILISAT ET SOLVANT POUR SOLUTION INJECTABLE

Authorised
  • Chorionic gonadotrophin
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Product identification

Medicine name:
CHORULON 5000 LYOPHILISAT ET SOLVANT POUR SOLUTION INJECTABLE
Active substance:
  • Chorionic gonadotrophin
Target species:
  • Cattle
  • Pig
  • Cat
  • Horse
  • Horse (mare)
  • Sheep
  • Goat
  • Dog
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Chorionic gonadotrophin
    1000.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Cat
    • Horse
      • Meat and offal
        0
        day
    • Horse (mare)
      • Milk
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Dog
  • Intravenous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Cat
    • Horse
      • Meat and offal
        0
        day
    • Horse (mare)
      • Milk
        0
        day
    • Sheep
      • Milk
        0
        day
      • All relevant tissues
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG03GA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Intervet
Marketing authorisation date:
Manufacturing sites for batch release:
  • INTERVET INTERNATIONAL B.V.
  • Intervet International GmbH
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/8336311 5/1983
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 30/10/2024
Download

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: 30/10/2024
Download
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