Veterinary Medicines

Genestran 75 micrograms/ml solution for injection for cattle, horses and pigs

Authorised
This information is not available for this product.
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Product identification

Medicine name:
Genestran 75 micrograms/ml solution for injection for cattle, horses and pigs
Genestran 75 mikrogramov/ml injekčný roztok pre hovädzí dobytok, kone a ošípané
Active substance:
This information is not available for this product.
Target species:
  • Cattle
  • Horse
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
This information is not available for this product.
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        1
        day
      • Milk
        0
        day
    • Horse
      • Meat and offal
        1
        day
    • Pig
      • Meat and offal
        1
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG02AD90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Package description:
  • Colourless vial of type I glass containing 20 ml of solution for injection, with chlorobutyl rubber stopper and aluminium cap.Presentation: Cardboard box of 1 vial of 20 ml
  • Colourless vial of type I glass containing 50 ml of solution for injection, with chlorobutyl rubber stopper and aluminium cap.Presentation: Cardboard box of 1 vial of 50 ml
  • Colourless vial of type I glass containing 20 ml of solution for injection, with chlorobutyl rubber stopper and aluminium cap.Presentation: Cardboard box of 5 vials of 20 ml

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Animedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Industrial Veterinaria S.A.
  • Animedica GmbH
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/027/MR/10-S
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0228/001
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • Estonia
  • France
  • Germany
  • Iceland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Slovak (PDF)
Published on: 3/02/2022
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Summary of Product Characteristics

English (PDF)
Published on: 11/02/2022
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