Ecomectin 5 mg/ml Pour-on Solution for Cattle
Ecomectin 5 mg/ml Pour-on Solution for Cattle
Authorised
- Ivermectin
Product identification
Medicine name:
Ecomectin 5 mg/ml Pour-on Solution for Cattle
Ecomectin 5 mg/ml pour-on oplossing Pour-on oplossing
Ecomectin 5 mg/ml solution pour pour-on Solution pour pour-on
Ecomectin 5 mg/ml Lösung zum Übergiessen Lösung zum übergiessen
Active substance:
- Ivermectin
Target species:
-
Cattle
Route of administration:
-
Pour-on use
Product details
Active substance and strength:
-
Ivermectin5.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Pour-on solution
Withdrawal period by route of administration:
-
Pour-on use
-
Cattle
-
Meat and offal31day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- 5.0 L white non-fluorinated or fluorinated high-density polyethylene back-pack with polypropylene strap and vented capClosure: White polypropylene screw-cap.
- 2.5 L white non-fluorinated or fluorinated high-density polyethylene back-pack with polypropylene strap and vented capClosure: White polypropylene screw-cap.
- 1.0 L white non-fluorinated or fluorinated high-density polyethylene bottle with a drawing tube and measuring device.Closure: White polypropylene screw-cap.
- 250 ml white non-fluorinated or fluorinated high-density polyethylene bottle with a drawing tube and measuring device.Closure: White polypropylene screw-cap.
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:
- Eco Animal Health Europe Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- ACME DRUGS
- Safapac Limited
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V226387
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0108/001
Concerned member states:
-
Belgium
-
France
-
Germany
-
Greece
-
Italy
-
Portugal
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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