Veterinary Medicines

Procamidor Duo 40 mg/ml + 0,036 mg/ml Injektionslösung für Tiere

Authorised
  • Procaine hydrochloride
  • EPINEPHRINE BITARTRATE
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Product identification

Medicine name:
Procamidor Duo 40 mg/ml + 0,036 mg/ml Injektionslösung für Tiere
Procamidor Comp. Vet. 40+0,036 mg/ml injektionsvæske, opløsning
Active substance:
  • Procaine hydrochloride
  • EPINEPHRINE BITARTRATE
Target species:
  • Cattle
  • Sheep
  • Horse
  • Pig
Route of administration:
  • Perineural use
  • Subcutaneous use

Product details

Active substance and strength:
  • Procaine hydrochloride
    40.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • EPINEPHRINE BITARTRATE
    0.04
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Perineural use
    • 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
  • Subcutaneous use
    • 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:
  • QN01BA52
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Denmark
Available in:
  • Denmark
Package description:
  • Amber glass vial type II (Ph. Eur.) with coated or uncoated bromobutyl rubber stopper type I (Ph.Eur.) and aluminium cap in a cardboard box. Cardboard box with 1 vial of 100 ml
  • Amber glass vial type II (Ph. Eur.) with coated or uncoated bromobutyl rubber stopper type I (Ph.Eur.) and aluminium cap in a cardboard box. Cardboard box with 1 vial of 250 ml
  • Amber glass vial type II (Ph. Eur.) with coated or uncoated bromobutyl rubber stopper type I (Ph.Eur.) and aluminium cap in a cardboard box. Cardboard box with 5 vials of 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:
  • Danish Medicines Agency
Authorisation number:
  • 60986
Date of authorisation status change:
Reference member state:
  • Austria
Procedure number:
  • AT/V/0018/001
Concerned member states:
  • Belgium
  • Bulgaria
  • Croatia
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

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Danish (, INJEKTIONSVÆSKE, OPLØSNING 40+0,036 MG-ML)
Published on: 29/06/2023
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