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ACEGON 50 mcg/ml solution for injection
  • Gonadorelin acetate
  • Valid
Authorised in these countries:
  • European Union
  • Poland

Product identification

Medicine name:
ACEGON 50 mcg/ml solution for injection
Acegon 50 mcg/1 ml + 50 mcg/1 ml Roztwór do wstrzykiwań
Active substance and strength:
  • Gonadorelin acetate
    50.00
    microgram(s)/millilitre
    /
    1.00
    millilitre(s)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01CA01
Authorisation number:
  • 2120
Product identification number:
  • 1a010a89-2a53-49d8-8212-10faf603c581
Permanent identification number:
  • 600000016890

Product details

Pharmaceutical form:
  • Solution for injection
Species grouped by route of administration:
  • Intramuscular use
    • Cattle (cow)
    • Cattle (heifer)

Availability

Package description:
  • cardboard box containing 10 vials of 6 ml
  • cardboard box containing 1 vial of 100 ml
  • cardboard box containing 1 vial of 50 ml
  • cardboard box containing 1 vial of 20 ml
  • cardboard box containing 1 vial of 6 ml
Manufacturing sites for batch release:
  • Syva
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:
  • ES/V/0158/001
Date of authorisation status change:
This information is not available for this product.
Authorisation country:
  • Poland
Responsible authority:
  • URPL
Marketing authorisation holder:
  • Syva
Marketing authorisation issued:
Reference member state:
  • Spain
Concerned member states:
  • Austria
  • Belgium
  • Cyprus
  • Czechia
  • France
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Slovakia
  • United Kingdom (Northern Ireland)
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

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