Veterinary Medicines

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

Authorised
  • Tulathromycin
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Product identification

Medicine name:
Huvexxin 100 mg/ml solution for injection for cattle, pigs and sheep
Huvexxin 100 mg/ml solution for injection for cattle, pigs and sheep
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:
  • Ireland
Package description:
  • Type I colourless glass vial with a chlorobutyl rubber stopper and an aluminium overseal. Pack sizes: Cardboard box containing one vial of 100 ml.
  • Type I colourless glass vial with a chlorobutyl rubber stopper and an aluminium overseal. Pack sizes: Cardboard box containing one vial of 20 ml.
  • Type I colourless glass vial with a chlorobutyl rubber stopper and an aluminium overseal. Pack sizes: Cardboard box containing one vial of 250 ml.
  • Type I colourless glass vial with a chlorobutyl rubber stopper and an aluminium overseal. Pack sizes: Cardboard box containing one vial of 50 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:
  • HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
  • Biovet J.S.C.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10782/040/002
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0662/002
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)
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