Insecinor 10 mg/ml Spot-on Solution for cattle and sheep
Insecinor 10 mg/ml Spot-on Solution for cattle and sheep
Authorised
- Deltamethrin
Product identification
Medicine name:
Insecinor 10 mg/ml Spot-on Solution for cattle and sheep
INSECINOR 10 MG/ML SOLUTION POUR SPOT-ON POUR BOVINS ET OVINS
Active substance:
- Deltamethrin
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Topical use
Product details
Active substance and strength:
-
Deltamethrin10.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Spot-on solution
Withdrawal period by route of administration:
-
Topical use
- Cattle
-
Meat and offal17day
-
Milk0hour
-
- Sheep
-
Meat and offal35day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53AC11
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- 2.5 litre white high density polyethylene back pack for use with a suitable dosing device and a white screw polypropylene cap in a cardboard box.
- 1 litre white high density polyethylene back pack for use with a suitable dosing device and a white screw polypropylene cap in a cardboard box.
- 500 ml clear high-density polyethylene bottle with internal graduated calibration chamber and a white screw polypropylene cap in a cardboard box.
- 250ml clear high-density polyethylene bottle with internal graduated calibration chamber and a white screw polypropylene cap in a cardboard box.
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:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Manufacturing Limited
Responsible authority:
- National Veterinary Medicines Agency
Authorisation number:
- FR/V/0013122 1/2014
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0545/001
Concerned member states:
-
Austria
-
France
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 11/02/2022
French (PDF)
Published on: 7/04/2022
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: 27/09/2023
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