Ecomectin 10 mg/ml Solution for Injection
Ecomectin 10 mg/ml Solution for Injection
Authorised
- Ivermectin
Product identification
Medicine name:
Ecomectin 10 mg/ml Solution for Injection
Active substance:
- Ivermectin
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Ivermectin10.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal49day
-
Milkno withdrawal periodDo not use in lactating cows producing milk for human consumption. Do not use in non-lactating dairy cows, including pregnant dairy heifers, within 60 days of calving.
-
-
Sheep
-
Meat and offal42day
-
Milkno withdrawal periodDo not use in lactating ewes producing milk for human consumption. Do not use in sheep which are intended to produce milk for human consumption within 60 days of lambing.
-
-
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:
-
Latvia
Package description:
- Clear PET multidose container with bromobutyl rubber stopper and aluminium cap. Pack size 250 ml
- HDPE multidose container with bromobutyl rubber stopper and aluminium cap.Pack size: 50 ml.
- HDPE multidose container with bromobutyl rubber stopper and aluminium cap.Pack size: 500 ml.
- HDPE multidose container with bromobutyl rubber stopper and aluminium cap.Pack size: 500 ml.
- HDPE multidose container with bromobutyl rubber stopper and aluminium cap.Pack size: 500 ml.
- HDPE multidose container with bromobutyl rubber stopper and aluminium cap.Pack size: 500 ml.
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:
- Produlab Pharma B.V.
- Divasa Farmavic S.A.
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/MRP/07/1684
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0144/001
Concerned member states:
-
Austria
-
Belgium
-
Estonia
-
France
-
Germany
-
Greece
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Latvian (PDF)
Published on: 5/10/2026
