Veterinary Medicines

Tullavis 100 mg/ml solution for injection for cattle, pigs and sheep

Authorised
  • Tulathromycin
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Product identification

Medicine name:
Tullavis 100 mg/ml solution for injection for cattle, pigs and sheep
TULLAVIS 100 MG/ML SOLUTION INJECTABLE POUR BOVINS, PORCINS, OVINS
Active substance:
  • Tulathromycin
Target species:
  • Sheep
  • Pig
  • Cattle
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Tulathromycin
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Sheep
      • Meat and offal
        16
        day
    • Pig
      • Meat and offal
        13
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        22
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01FA94
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Package description:
  • Clear glass (Type II Ph. Eur.) vial closed with a bromobutyl rubber stopper and sealed with an aluminium cap.Cardboard box containing 1 vial of 250 ml.
  • Clear glass (Type II Ph. Eur.) vial closed with a bromobutyl rubber stopper and sealed with an aluminium cap.Cardboard box containing 1 vial of 100 ml.
  • Clear glass (Type II Ph. Eur.) vial closed with a bromobutyl rubber stopper and sealed with an aluminium cap.Cardboard box containing 1 vial of 50 ml.
  • Clear glass (Type II Ph. Eur.) vial closed with a bromobutyl rubber stopper and sealed with an aluminium cap.Cardboard box containing 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:
  • Industrial Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • aniMedica Herstellungs GmbH
  • aniMedica Herstellungs GmbH
  • Industrial Veterinaria S.A.
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/2318291 4/2020
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0893/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 9/11/2025
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French (PDF)
Published on: 8/12/2022
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Combined File of all Documents

English (PDF)
Published on: 9/11/2025
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Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 27/11/2025
Download

eu-PUAR-esv0358001-dcp-tulavis-100-mg-mlsolution-for-injection-for-cattle--pigs-and-sheep-en.pdf

English (PDF)
Published on: 21/12/2023
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