Intermectin Injection 10 mg/ml solution for injection for cattle, sheep and pigs
Intermectin Injection 10 mg/ml solution for injection for cattle, sheep and pigs
Authorised
- Ivermectin
Product identification
Medicine name:
Intermectin Injection 10 mg/ml solution for injection for cattle, sheep and pigs
Intermectin injection, 10mg/ml, Injekční roztok
Active substance:
- Ivermectin
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Ivermectin10.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal49day
-
-
Sheep
-
Meat and offal63day
-
-
Pig
-
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
Package description:
- Clear glass bottles (type II) closed with a bromobutyl rubber stopper and sealed with an aluminium cap packed into an outer cardboard box
- Clear glass bottles (type II) closed with a bromobutyl rubber stopper and sealed with an aluminium flip-off cap with polypropylene cover packed into an outer cardboard box
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Interchemie Werken De Adelaar B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Interchemie Werken De Adelaar Eesti AS
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/005/25-C
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0431/001
Concerned member states:
-
Austria
-
Croatia
-
Cyprus
-
Czechia
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Malta
-
Portugal
-
Slovakia
-
Slovenia
-
Spain
Generic of:
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: 7/02/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 7/02/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 7/02/2025
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