Veterinary Medicines

GESLIN

Authorised
  • Buserelin acetate
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Product identification

Medicine name:
GESLIN
Geslin 0,004 mg/ml Roztwór do wstrzykiwań
Active substance:
  • Buserelin acetate
Target species:
  • Cattle (cow)
  • Pig (sow for reproduction)
  • Horse (mare)
  • Rabbit (female for reproduction)
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Buserelin acetate
    0.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle (cow)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig (sow for reproduction)
      • Meat and offal
        0
        day
    • Horse (mare)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Rabbit (female for reproduction)
      • Meat and offal
        0
        day
  • Intravenous use
    • Cattle (cow)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig (sow for reproduction)
      • Meat and offal
        0
        day
    • Horse (mare)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Rabbit (female for reproduction)
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Cattle (cow)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig (sow for reproduction)
      • Meat and offal
        0
        day
    • Horse (mare)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Rabbit (female for reproduction)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01CA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Available in:
  • Poland
Package description:
  • Box with 5 vials of 20 ml
  • Box with 1 vial of 20 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:
  • Mevet S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Mevet S.A.
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 3302
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0434/001
Concerned member states:
  • Cyprus
  • Estonia
  • Poland
  • Romania

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 25/10/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 25/10/2024
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 25/10/2024
Download

Combined File of all Documents

English (PDF)
Published on: 24/07/2025
Download