VERMAX D
VERMAX D
Authorised
- Ivermectin
- Closantel sodium dihydrate
Product identification
Medicine name:
VERMAX D
Active substance:
- Ivermectin
- Closantel sodium dihydrate
Target species:
-
Sheep
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Ivermectin50.00/milligram(s)1.00millilitre(s)
-
Closantel sodium dihydrate135.90/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Sheep
-
Meat and offal28day
-
Milkno withdrawal periodNe pas administrer chez les brebis laitières productrices de lait destiné à la consommation humaine, y compris pendant la période de tarissement. Ne pas utiliser dans la période d'un an précédant le premier agnelage chez les brebis destinées à la production de lait pour la consommation humaine.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent application (Article 13c of Directive No 2001/82/EC)
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/9829328 1/2010
Date of authorisation status change:
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: 6/03/2023
