Veterinary Medicines

Xylamidor 20 mg/ml Injektionslösung für Tiere

Authorised
  • Xylazine hydrochloride
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Product identification

Medicine name:
Xylamidor 20 mg/ml Injektionslösung für Tiere
Xylamidor 20 mg/ml Injektionslösung für Rinder, Pferde, Hunde und Katzen
Active substance:
  • Xylazine hydrochloride
Target species:
  • Cattle
  • Dog
  • Cat
  • Horse
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Xylazine hydrochloride
    23.32
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        1
        day
      • Milk
        0
        hour
    • Dog
    • Cat
  • Intravenous use
    • Cattle
      • Meat and offal
        1
        day
      • Milk
        0
        hour
    • Dog
    • Horse
      • Meat and offal
        1
        day
      • Milk
        0
        hour
  • Subcutaneous use
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN05CM92
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Package description:
  • Clear glass vial type I with 5 x 10 ml solution for injection with a coated bromobutyl rubber stopper, type I and aluminium cap in a cardboard box.
  • Clear glass vial type II with 25 ml solution for injection with a coated bromobutyl rubber stopper, type I and aluminium cap.
  • Clear glass vial type II with 50 ml solution for injection with a coated bromobutyl rubber stopper, type I and aluminium cap.
  • Clear glass vial type I with 10 ml solution for injection with a coated bromobutyl rubber stopper, type I and aluminium cap.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 18 of Regulation (EU) 2019/6)
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:
  • V7009313.00.00
Date of authorisation status change:
Reference member state:
  • Austria
Procedure number:
  • AT/V/0029/001
Concerned member states:
  • Belgium
  • Bulgaria
  • Cyprus
  • Denmark
  • Finland
  • France
  • Germany
  • Greece
  • Ireland
  • Italy
  • Latvia
  • Netherlands
  • Norway
  • Poland
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
Generic of:

Documents

Combined File of all Documents

English (PDF)
Published on: 22/12/2023
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German (PDF)
Published on: 20/12/2024
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