Veterinary Medicines

Procaine HCl 2 % Oplossing voor injectie

Not authorised
  • Procaine hydrochloride
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Product identification

Medicine name:
Procaine HCl 2 % Oplossing voor injectie
Procaine HCl 2 % Solution injectable
Procaine HCl 2 % Injektionslösung
Active substance:
  • Procaine hydrochloride
Target species:
  • Sheep
  • Cattle
  • Pig
  • Dog
  • Horse
  • Cat
Route of administration:
  • Epidural use
  • Subcutaneous use
  • Perineural use

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
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01BA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Belgium
Package description:
  • Procaine HCl 12 Vials with 500 ml of Solution for injection
  • Procaine HCl 12 Vials with 250 ml of Solution for injection
  • Procaine HCl 12 Vials with 100 ml of Solution for injection
  • Procaine HCl 12 Vials with 50 ml of Solution for injection
  • Procaine HCl 1 Vial with 500 ml of Solution for injection
  • Procaine HCl 1 Vial with 250 ml of Solution for injection
  • Procaine HCl 1 Vial with 100 ml of Solution for injection
  • Procaine HCl 1 Vial with 50 ml of Solution for injection

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
  • VMD N.V.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V104361
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 22/03/2022
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French (PDF)
Published on: 22/03/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 22/03/2022
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French (PDF)
Published on: 22/03/2022
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German (PDF)
Published on: 22/03/2022
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