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Folligon 1000 S.V. liofilizāts un šķīdinātājs šķīduma injekcijām pagatavošanai liellopiem, cūkām, kazām, aitām, trušiem, briežiem un ūdelēm

Not authorised
  • Gonadotropin, equine, serum
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Product identification

Medicine name:
Folligon 1000 S.V. liofilizāts un šķīdinātājs šķīduma injekcijām pagatavošanai liellopiem, cūkām, kazām, aitām, trušiem, briežiem un ūdelēm
Active substance:
  • Gonadotropin, equine, serum
Target species:
  • Pig
  • Rabbit
  • Mink
  • Cattle
  • Sheep
  • Goat
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Gonadotropin, equine, serum
    1000.00
    international unit(s)
    /
    1.00
    Vial
Pharmaceutical form:
  • Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        0
        day
    • Rabbit
      • Meat and offal
        0
        day
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Rabbit
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG03GA03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Latvia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
  • Intervet International GmbH
Responsible authority:
  • Food And Veterinary Service
Authorisation number:
  • V/NRP/02/1468
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.
Latvian (PDF)
Published on: 24/10/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 24/10/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 24/10/2025
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