Veterinary Medicines

Gentamycin 85 mg/ ml šķīdums injekcijām liellopiem, cūkām, zirgiem, suņiem un kaķiem

Authorised
  • Gentamicin sulfate
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Product identification

Medicine name:
Gentamycin 85 mg/ ml šķīdums injekcijām liellopiem, cūkām, zirgiem, suņiem un kaķiem
Active substance:
  • Gentamicin sulfate
Target species:
  • Horse (non food-producing)
  • Cattle (calf)
  • Pig (piglet)
  • Pig (weaned piglet)
  • Dog
  • Cat
  • Cattle
Route of administration:
  • Intravenous use
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Gentamicin sulfate
    85.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Horse (non food-producing)
    • Cattle (calf)
      • Meat and offal
        192
        day
    • Pig (piglet)
      • Meat and offal
        146
        day
    • Pig (weaned piglet)
      • Meat and offal
        146
        day
    • Dog
    • Cat
    • Cattle
      • Meat and offal
        214
        day
      • Milk
        7
        day
  • Intramuscular use
    • Cattle
      • Meat and offal
        214
        day
      • Milk
        7
        day
    • Cattle (calf)
      • Meat and offal
        192
        day
    • Pig (piglet)
      • Meat and offal
        146
        day
    • Pig (weaned piglet)
      • Meat and offal
        146
        day
    • Cat
    • Dog
  • Subcutaneous use
    • Dog
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01GB03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Latvia
Available 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:
  • Bela-Pharm GmbH & Co. KG
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bela-Pharm GmbH & Co. KG
Responsible authority:
  • Food And Veterinary Service
Authorisation number:
  • V/NRP/95/0110
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: 27/02/2024
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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: 27/02/2024
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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: 27/02/2024
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