Veterinary Medicine Information website

Doramax 5 mg/ml Pour-on Solution for Cattle

Authorised
  • Doramectin
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Product identification

Medicine name:
Doramax 5 mg/ml Pour-on Solution for Cattle
Active substance:
  • Doramectin
Target species:
  • Cattle
Route of administration:
  • Pour-on use

Product details

Active substance and strength:
  • Doramectin
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Pour-on solution
Withdrawal period by route of administration:
  • Pour-on use
    • Cattle
      • Meat and offal
        35
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AA03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Package description:
  • The product will be supplied in:8L (5 L + 3 L) high-density polyethylene bottles with a tamper evident cap in a carton box
  • The product will be supplied in:6L (5L+1L) high-density polyethylene bottles with a tamper evident cap in a carton box
  • The product will be supplied in:5 L high-density polyethylene bottles with a tamper evident cap in a carton box
  • The product will be supplied in:3 L high-density polyethylene bottles with a tamper evident cap in a carton box
  • The product will be supplied in:2.5 L high-density polyethylene bottles with a tamper evident cap in a carton box
  • The product will be supplied in:1 L high-density polyethylene bottles with a tamper evident cap in a carton box

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • V7007518.00.00
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0669/001
Concerned member states:
  • Belgium
  • Czechia
  • France
  • Germany
  • Hungary
  • Netherlands
  • Poland
  • Romania
  • Slovenia

Documents

Combined File of all Documents

English (PDF)
Published on: 15/02/2026
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German (PDF)
Published on: 10/01/2025
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Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
Updated on: 13/03/2026
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