Ivomec vet. 0,8 mg/ml, mikstur oppløsning
Ivomec vet. 0,8 mg/ml, mikstur oppløsning
Authorised
- Ivermectin
Product identification
Medicine name:
Ivomec vet. 0,8 mg/ml, mikstur oppløsning
Active substance:
- Ivermectin
Target species:
-
Sheep
-
Goat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Ivermectin0.80/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral solution
Withdrawal period by route of administration:
-
Oral use
-
Sheep
-
Meat and offal6daySows and goats that produce milk for human consumption cannot be treated during lactation or within 28 days before lactation.
-
-
Goat
-
Meat and offal8daySows and goats that produce milk for human consumption cannot be treated during lactation or within 28 days before lactation.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Norway
Available in:
-
Norway
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health Denmark A/S
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Norwegian Medical Products Agency
Authorisation number:
- 0000-07737
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.
Norwegian (PDF)
Published on: 2/07/2024
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Norwegian (PDF)
Published on: 2/07/2024
