Veterinary Medicines

Mepidor 20 mg/ml Solution for Injection

Authorised
  • Mepivacaine hydrochloride
  • Mepivacaine hydrochloride
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Product identification

Medicine name:
Mepidor 20 mg/ml solution for injection
Mepidor 20 mg/ml Solution for Injection
Active substance:
  • Mepivacaine hydrochloride
  • Mepivacaine hydrochloride
Target species:
  • Horse (non food-producing)
  • Horse
Route of administration:
  • Infiltration
  • Epidural use
  • Intraarticular use

Product details

Active substance and strength:
  • Mepivacaine hydrochloride
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Mepivacaine hydrochloride
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Infiltration
    • Horse (non food-producing)
  • Epidural use
    • Horse
  • Intraarticular use
    • Horse
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01BB03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • United Kingdom (Northern Ireland)
Available in:
  • United Kingdom (Northern Ireland)
Package description:
  • Cardboard box with clear glass vials type I, 6X10 ml, bromobutyl rubber stopper or bromobutyl stopper with a fluorinated polymer coating and aluminium cap.
  • Cardboard box with clear glass vials type I, 10 ml, bromobutyl rubber stopper or bromobutyl stopper with a fluorinated polymer coating and aluminium cap.
  • Cardboard box with clear glass vials type I, 5X10 ml, bromobutyl rubber stopper or bromobutyl stopper with a fluorinated polymer coating and aluminium cap.

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:
  • Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Richter Pharma AG
Responsible authority:
  • The Veterinary Medicines Directorate
Authorisation number:
  • Vm 22080/4008
Date of authorisation status change:
Reference member state:
  • Portugal
Procedure number:
  • PT/V/0128/001
Concerned member states:
  • Belgium
  • Iceland
  • Italy
  • Norway
  • United Kingdom (Northern Ireland)
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