Veterinary Medicines

Depedin suspensija injekcijām zirgiem, liellopiem, cūkām, suņiem un kaķiem

Authorised
  • Prednisolone acetate
  • Dexamethasone
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Product identification

Medicine name:
Depedin suspensija injekcijām zirgiem, liellopiem, cūkām, suņiem un kaķiem
Active substance:
  • Prednisolone acetate
  • Dexamethasone
Target species:
  • Horse
  • Cattle
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Prednisolone acetate
    7.50
    milligram(s)
    /
    1.00
    millilitre(s)
  • Dexamethasone
    2.50
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Horse
      • Meat and offal
        8
        day
      • Milk
        no withdrawal period
    • Cattle
      • Meat and offal
        8
        day
      • Milk
        24
        hour
    • Pig
      • Meat and offal
        6
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH02AB30
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
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:
  • Veyx Pharma GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Veyx Pharma GmbH
  • Veyx-Pharma B.V.
Responsible authority:
  • Food And Veterinary Service
Authorisation number:
  • V/NRP/92/0216
Date of authorisation status change:

Documents

Labelling

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Latvian (PDF)
Published on: 17/09/2025
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Summary of Product Characteristics

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Latvian (PDF)
Published on: 17/09/2025
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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: 17/09/2025
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