Adrenaline 1 mg/ml, oplossing voor injectie
  • Adrenaline hydrogen tartrate
  • Valid
Authorised in these countries:
  • Netherlands
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Product identification

Medicine name:
Adrenaline 1 mg/ml, oplossing voor injectie
Active substance and strength:
  • Adrenaline hydrogen tartrate
    1.80
    milligram(s)
    /
    1.00
    millilitre(s)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QC01CA24
Authorisation number:
  • REG NL 5075
Product identification number:
  • 9021d043-4bde-46f0-8435-9787af965a7b
Permanent identification number:
  • 600000079599

Product details

Legal status of supply:
This information is not available for this product.
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
      • Meat and offal
        1
        day
    • Goat (adult female)
      • Milk
      • Meat and offal
        1
        day
    • Sheep
      • Milk
      • Meat and offal
        1
        day
    • Horse
      • Meat and offal
        1
        day
    • Pig
      • Meat and offal
        1
        day
    • Dog
    • Cat
  • Subcutaneous use
    • Cattle
      • Milk
      • Meat and offal
        1
        day
    • Goat (adult female)
      • Milk
      • Meat and offal
        1
        day
    • Sheep
      • Milk
      • Meat and offal
        1
        day
    • Horse
      • Meat and offal
        1
        day
    • Pig
      • Meat and offal
        1
        day
    • Dog
    • Cat

Availability

Package description:
Manufacturing sites for batch release:
  • Alfasan Nederland B.V.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
This information is not available for this product.
Date of authorisation status change:
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Authorisation country:
  • Netherlands
Responsible authority:
  • Medicines Evaluation Board
Marketing authorisation holder:
  • Alfasan Nederland B.V.
Marketing authorisation issued:
Reference member state:
This information is not available for this product.
Concerned member states:
This information is not available for this product.
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Combined File of all Documents (PDF)
First published:
Last updated:
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