Veterinary Medicines

Econor Surrendered - 1% - Premix for medicated feeding stuff

Authorised
  • Valnemulin
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Product identification

Medicine name:
Econor Surrendered - 1% - Premix for medicated feeding stuff
Active substance:
  • Valnemulin
Target species:
  • Pig
Route of administration:
  • In-feed use

Product details

Active substance and strength:
  • Valnemulin
    10.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Premix for medicated feeding stuff
Withdrawal period by route of administration:
  • In-feed use
    • Pig
      • Meat and offal
        1
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01XQ02
Legal status of supply:
  • Medicinal product subject to medical prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)
Package description:
  • Packaging:LDPE bags in cardboard outers, Package_size:1 bag, Content:1 kg, Qualifier:1 g valnemulin base per 100 g
  • Packaging:Aluminum lined plastic bag, Package_size:1 bag, Content:25 kg, Qualifier:1 g valnemulin base per 100 g
  • Packaging:Aluminum lined plastic bag, Package_size:1 bag, Content:2.5 kg, Qualifier:1 g valnemulin base per 100 g
  • Packaging:Aluminum lined plastic bag, Package_size:1 bag, Content:1 kg, Qualifier:1 g valnemulin base per 100 g
  • Packaging:LDPE bags in cardboard outers, Package_size:1 bag, Content:25 kg, Qualifier:1 g valnemulin base per 100 g
  • Packaging:LDPE bags in cardboard outers, Package_size:1 bag, Content:2.5 kg, Qualifier:1 g valnemulin base per 100 g

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Elanco GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Sandoz GmbH
Responsible authority:
  • European Commission
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
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