Ecomectin 10 mg/ml Solution for Injection
  • Ivermektīns
  • Valid
Authorised in these countries:
  • France
Export to PDF

Product identification

Medicine name:
Ecomectin 10 mg/ml Solution for Injection
VETOMECTIN 10 MG/ML SOLUTION INJECTABLE
Active substance and strength:
  • Ivermektīns
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AA01
Authorisation number:
  • FR/V/4934184 5/2004
Product identification number:
  • 72b3679f-5db4-462d-be62-f06590f6ddb4
Permanent identification number:
  • 600000048722

Product details

Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        42
        day
    • Sheep
      • Meat and offal
        42
        day
    • Pig
      • Meat and offal
        28
        day

Availability

Package description:
  • Clear PET 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: 200 ml.
  • Clear PET 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: 50 ml.
  • Clear PET multidose container with bromobutyl rubber stopper and aluminium cap. Pack size 250 ml
Manufacturing sites for batch release:
  • Produlab Pharma B.V.
  • Divasa Farmavic S.A.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
  • IE/V/0144/001
Date of authorisation status change:
Legal basis of product authorisation:
  • Well-established use application (Article 13a of Directive No 2001/82/EC)
Authorisation country:
  • France
Responsible authority:
  • ANSES
Marketing authorisation holder:
  • Eco Animal Health Europe Limited
Marketing authorisation issued:
Reference member state:
  • Ireland
Concerned member states:
  • Austria
  • Belgium
  • Estonia
  • France
  • Germany
  • Greece
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Portugal
  • Spain
  • United Kingdom (Northern Ireland)
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Summary of Product Characteristics (PDF)
First published:
Last updated:
Summary of Product Characteristics (PDF)
First published:
Last updated:
Package Leaflet and Labelling (PDF)
First published:
Last updated:
Package Leaflet and Labelling (PDF)
First published:
Last updated:
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."