Veterinary Medicines

Folligon PMSG 1000 UI lyophilisat et solvant pour solution injectable

Authorised
  • Serum gonadotrophin
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Product identification

Medicine name:
Folligon PMSG 1000 UI lyophilisat et solvant pour solution injectable
Folligon PMSG 1000 IU Lyophilisat und Lösungsmittel zur Herstellung einer Injektionssuspension
Active substance:
  • Serum gonadotrophin
Target species:
  • Sheep
  • Rabbit
  • Horse
  • Pig
  • Goat
  • Cattle
  • Dog
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Serum gonadotrophin
    1000.00
    international unit(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Sheep
      • Meat and offal, milk
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal, milk
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
    • Goat
      • Meat and offal, milk
        no withdrawal period
    • Cattle
      • Meat and offal, milk
        no withdrawal period
  • Subcutaneous use
    • Horse
      • Meat and offal, milk
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG03GA99
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Luxembourg
Available in:
  • Luxembourg
Package description:
  • 1 Vial with 1000 IU of Lyophilisate and 1 Vial of 1 dose of solvent for suspension for injection

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International GmbH
Responsible authority:
  • Ministry Of Health And Social Security
Authorisation number:
  • V 817/09/07/1469
Date of authorisation status change:

Documents

Summary of Product Characteristics

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French (PDF)
Published on: 14/08/2023
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