IVERMIX, 0,15mg/g, Perorální prášek
IVERMIX, 0,15mg/g, Perorální prášek
Authorised
- Ivermectin
Product identification
Medicine name:
IVERMIX, 0,15mg/g, Perorální prášek
Active substance:
- Ivermectin
Target species:
-
Fallow deer
-
Roe deer
-
Mouflon
-
Wild boar
-
Red deer
Route of administration:
-
In-feed use
Product details
Active substance and strength:
-
Ivermectin0.15/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
In-feed use
-
Fallow deer
-
Meat and offal28day
-
-
Roe deer
-
Meat and offal28day
-
-
Mouflon
-
Meat and offal28day
-
-
Wild boar
-
Meat and offal14day
-
-
Red deer
-
Meat and offal28day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Tekro spol. s r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Tekro spol. s r.o.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/096/11-C
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.
Czech (PDF)
Published on: 26/10/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 26/10/2022
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 26/10/2022
