Veterinary Medicines

ULTRADIAZINE

Authorised
  • Sulfadiazine sodium
  • Trimethoprim
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Product identification

Medicine name:
ULTRADIAZINE
Active substance:
  • Sulfadiazine sodium
  • Trimethoprim
Target species:
  • Cattle
  • Sheep
  • Goat
  • Pig (for fattening)
  • Pig (piglet)
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Sulfadiazine sodium
    217.58
    milligram(s)
    /
    1.00
    millilitre(s)
  • Trimethoprim
    40.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        no withdrawal period
    • Sheep
      • Meat and offal
        no withdrawal period
    • Goat
      • Meat and offal
        no withdrawal period
    • Pig (for fattening)
      • Meat and offal
        no withdrawal period
    • Pig (piglet)
      • Meat and offal
        no withdrawal period
    • Sheep
      • Milk
        no withdrawal period
    • Goat
      • Milk
        no withdrawal period
  • Intravenous use
    • Cattle
      • Meat and offal
        no withdrawal period
    • Sheep
      • Meat and offal
        no withdrawal period
    • Goat
      • Meat and offal
        no withdrawal period
    • Pig (for fattening)
      • Meat and offal
        no withdrawal period
    • Pig (piglet)
      • Meat and offal
        no withdrawal period
    • Cattle
      • Milk
        no withdrawal period
    • Sheep
      • Milk
        no withdrawal period
    • Goat
      • Milk
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01EW10
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Spain
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • S P Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • S P Veterinaria S.A.
Responsible authority:
  • Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 857 ESP
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Spanish (PDF)
Published on: 8/11/2022
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Package Leaflet

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Spanish (PDF)
Published on: 8/11/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 8/11/2022
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