Veterinary Medicines

Procamidor 20 mg/ml - Injektionslösung für Tiere

Authorised
  • Procaine hydrochloride
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Product identification

Medicine name:
Procamidor 20 mg/ml - Injektionslösung für Tiere
Procamidor vet. 20 mg/ml injeksjonsvæske, oppløsning
Active substance:
  • Procaine hydrochloride
Target species:
  • Cattle
  • Dog
  • Sheep
  • Pig
  • Cat
  • Horse
Route of administration:
  • Epidural use
  • Perineural use
  • Infiltration

Product details

Active substance and strength:
  • Procaine hydrochloride
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Epidural use
    • Cattle
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • Infiltration
    • Cattle
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Horse
      • Milk
        0
        hour
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01BA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Norway
Available in:
  • Norway
Package description:
  • Clear glass vial type II (Ph. Eur.) with bromobutyl rubber stopper type I (Ph.Eur.) and aluminium cap. Package sizes 10 x 100 ml
  • Clear glass vial type II (Ph. Eur.) with bromobutyl rubber stopper type I (Ph.Eur.) and aluminium cap. Package size: 1 x 100 ml

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:
  • Vetviva Richter GmbH
Responsible authority:
  • Norwegian Medical Products Agency
Authorisation number:
  • 13-9613
Date of authorisation status change:
Reference member state:
  • Austria
Procedure number:
  • AT/V/0011/001
Concerned member states:
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Iceland
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Norway
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Norwegian (PDF)
Published on: 9/04/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Norwegian (PDF)
Published on: 9/04/2025
Download