Intermec Drench, 0,8 mg/ml suukaudne lahus lammastele
Intermec Drench, 0,8 mg/ml suukaudne lahus lammastele
Authorised
- Ivermectin
Product identification
Medicine name:
Intermec Drench, 0,8 mg/ml suukaudne lahus lammastele
Active substance:
- Ivermectin
Target species:
-
Sheep
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 offal6day
-
Milkno withdrawal periodPiimale: ei ole lubatud kasutamiseks lammastel, kelle piima tarvitatakse inimtoiduks. Mitte kasutada 28 päeva enne oodatavat poegimist nendel tiinetel lammastel, kelle piima kavatsetakse tarvitada inimtoiduks.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Estonia
Package description:
- Available only in Estonian
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:
- Interchemie Werken De Adelaar Eesti AS
Marketing authorisation date:
Manufacturing sites for batch release:
- Interchemie Werken De Adelaar Eesti AS
Responsible authority:
- State Agency Of Medicines
Authorisation number:
- 2138
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.
Estonian (PDF)
Published on: 27/11/2024
