Veterinary Medicines

Adrilan 1 mg/ml solução injectável

Authorised
  • ADRENALINE
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Product identification

Medicine name:
Adrilan 1 mg/ml solução injectável
Active substance:
  • ADRENALINE
Target species:
  • Dog
  • Horse
  • Cattle
  • Sheep
  • Cat
  • Ornamental bird
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Intracardiac use
  • Subcutaneous use

Product details

Active substance and strength:
  • ADRENALINE
    1.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Dog
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
    • Cattle
      • Meat and offal, milk
        0
        day
    • Sheep
      • Meat and offal, milk
        0
        day
  • Intravenous use
    • Dog
      • Meat and offal
        0
        day
    • Cat
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
    • Cattle
      • Meat and offal, milk
        0
        day
    • Sheep
      • Meat and offal, milk
        0
        day
    • Ornamental bird
      • Meat and offal
        0
        day
  • Intracardiac use
    • Dog
      • Meat and offal
        0
        day
    • Cat
      • Meat and offal
        0
        day
    • Ornamental bird
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Dog
      • Meat and offal
        0
        day
    • Cat
      • Meat and offal
        0
        day
    • Cattle
      • Meat and offal, milk
        0
        day
    • Horse
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal, milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QR03AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Package description:

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:
  • Medinfar Serological Products And Equipment S.A.
Marketing authorisation issued:
Manufacturing sites for batch release:
  • Labesfal Laboratorios Almiro S.A.
Authorisation country:
  • Portugal
Responsible authority:
  • DGAV
Authorisation number:
  • 51322
Date of authorisation status change:

Documents

Combined File of all Documents

Published:
Portuguese (PDF)
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