Veterinary Medicines

VeteCorH 1000 IU/ml lyophilizate and solvent for solution for injection for cattle, horses, sheep, goats, pigs, cats and dogs

Authorised
  • HUMAN CHORIONIC GONADOTROPIN
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Product identification

Medicine name:
VETECORH 1000 IU/ML LYOPHILISATE AND SOLVENT FOR SOLUTION FOR INJECTION FOR CATTLE, HORSES, SHEEP, GOATS, PIGS, CATS AND DOGS
VeteCorH 1000 IU/ml lyophilizate and solvent for solution for injection for cattle, horses, sheep, goats, pigs, cats and dogs
Active substance:
  • HUMAN CHORIONIC GONADOTROPIN
Target species:
  • Cattle
  • Pig
  • Cat
  • Horse
  • Sheep
  • Goat
  • Dog
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • HUMAN CHORIONIC GONADOTROPIN
    5000.00
    international unit(s)
    /
    1.00
    Bottle
Pharmaceutical form:
  • Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        day
  • Intravenous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG03GA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • Box of 1 vial of lyophilisate + Box of 1 vial of 5 ml of solvent
  • Box of 2 vials of lyophilisate + Box of 2 vials of 5 ml of solvent
  • Box of 5 vials of lyophilisate + Box of 5 vials of 5 ml of solvent
  • Box of 1 vial of lyophilisate and 1 vial 5 ml of solvent
  • Box of 2 vials of lyophilisate and 2 vials 5 ml of solvent
  • Box of 5 vials of lyophilisate and 5 vials of 5 ml of solvent

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application - change in active substance(s) (Article 19(1)(a) of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Laboratorios Calier S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratorios Calier S.A.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10665/010/001
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0467/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Germany
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Spain
  • United Kingdom (Northern Ireland)