Taurador 10 mg/ml Solution for Injection for cattle, sheep & pigs
Taurador 10 mg/ml Solution for Injection for cattle, sheep & pigs
Authorised
- Doramectin
Product identification
Medicine name:
Taurador 10 mg/ml Solution for Injection for cattle, sheep & pigs
TAURADOR 10 MG/ML SOLUTION INJECTABLE POUR BOVINS, OVINS ET PORCINS
Active substance:
- Doramectin
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Doramectin10.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal70day
-
Milkno withdrawal periodNot authorised for use in animals producing milk for human consumption. Do not use in pregnant cows or heifers which are intended to produce milk for human consumption within 2 months of expected parturition.
-
-
-
Intramuscular use
-
Sheep
-
Meat and offal70day
-
Milkno withdrawal periodNot authorised for use in animals producing milk for human consumption. Do not use in pregnant ewes which are intended to produce milk for human consumption within 70 days of expected parturition.
-
-
Pig
-
Meat and offal77day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- (ID3) 500 millilitre(s): Behältnis (Plastic) with 1 Vial (Glass) with 500 millilitre(s), closed with Stopper and Lid (Rubber, Aluminium)
- (ID2) 250 millilitre(s): Behältnis (Plastic) with 1 Vial (Glass) with 250 millilitre(s), closed with Lid and Stopper (Aluminium, Rubber)
- (ID1) 100 millilitre(s): Behältnis (Plastic) with 1 Vial (Glass) with 100 millilitre(s), closed with Stopper and Lid (Rubber, Aluminium)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Manufacturing Limited
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/9608288 5/2024
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0345/001
Concerned member states:
-
Belgium
-
Czechia
-
France
-
Hungary
-
Ireland
-
Netherlands
-
Portugal
-
Romania
-
Slovakia
-
Spain
Generic of:
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.
French (PDF)
Published on: 17/12/2024
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: 15/10/2025
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