Huvexxin 100 mg/ml solution for injection for cattle, pigs and sheep
Huvexxin 100 mg/ml solution for injection for cattle, pigs and sheep
Authorised
- Tulathromycin
Product identification
Medicine name:
Huvexxin 100 mg/ml Solution injectable
Huvexxin 100 mg/ml Injektionslösung
Huvexxin 100 mg/ml Oplossing voor injectie
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:
-
Tulathromycin100.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Sheep
-
Meat and offal16day
-
- Pig
-
Meat and offal13day
-
-
Subcutaneous use
- Cattle
-
Meat and offal22day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01FA94
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
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:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V660939
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)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
How useful was this page?: