Veterinary Medicines

Adrenaline, 1 mg/ml oplossing voor injectie

Authorised
  • Epinephrine
Download as PDF

Product identification

Medicine name:
Adrenaline, 1 mg/ml oplossing voor injectie
Active substance:
  • Epinephrine
Target species:
  • Cattle
  • Sheep
  • Horse
  • Pig
  • Dog
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Epinephrine
    1.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        no withdrawal period
      • Meat and offal
        1
        day
    • Sheep
      • Milk
        no withdrawal period
      • Meat and offal
        1
        day
    • Horse
      • Meat and offal
        1
        day
    • Pig
      • Meat and offal
        1
        day
    • Dog
  • Intravenous use
    • Cattle
      • Milk
        no withdrawal period
      • Meat and offal
        1
        day
    • Sheep
    • Horse
      • Meat and offal
        1
        day
    • Pig
    • Dog
  • Subcutaneous use
    • Cattle
      • Milk
        no withdrawal period
      • Meat and offal
        1
        day
    • Sheep
      • Milk
        no withdrawal period
      • Meat and offal
        1
        day
    • Horse
      • Meat and offal
        1
        day
    • Pig
      • Meat and offal
        1
        day
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QC01CA24
Legal status of supply:
  • Medicinal product subject to medical prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Alfasan Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Kela - Kempisch Laboratorium - Kela Laboratoria
Responsible authority:
  • MEB
Authorisation number:
  • REG NL 4756
Date of authorisation status change:

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 23/02/2022
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."