Veterinary Medicines

Mepidor 20 mg/ml solution for injection for horses

Authorised
  • Mepivacaine hydrochloride
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Product identification

Medicine name:
Mepidor 20 mg/ml solution for injection for horses
Mepidor 20 mg/ml Injektionslösung für Pferde
Active substance:
  • Mepivacaine hydrochloride
Target species:
  • Horse
Route of administration:
  • Epidural use
  • Intraarticular use

Product details

Active substance and strength:
  • Mepivacaine hydrochloride
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Epidural use
    • Horse
      • Meat and offal
        3
        day
      • Milk
        72
        hour
  • Intraarticular use
    • Horse
      • Meat and offal
        3
        day
      • Milk
        72
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01BB03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:
  • Cardboard box with clear glass vial type I, bromobutyl rubber stopper or bromobutyl stopper with a fluorinated polymer coating and aluminium capPack sizes: 10 ml.
  • Cardboard box with clear glass vial type I, bromobutyl rubber stopper or bromobutyl stopper with a fluorinated polymer coating and aluminium capPack sizes: 5 x 10 ml.
  • Cardboard box with clear glass vial type I, bromobutyl rubber stopper or bromobutyl stopper with a fluorinated polymer coating and aluminium capPack sizes: 6 x 10 ml.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetviva Richter GmbH
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 402411.00.00
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0425/001
Concerned member states:
  • Austria
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Netherlands
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 23/11/2025
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Combined File of all Documents

English (PDF)
Published on: 23/11/2025
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German (PDF)
Published on: 26/01/2026
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