Veterinary Medicines

LongActon 0.07 mg/ml solution for injection for cattle and pigs

Authorised
  • Carbetocin
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Product identification

Medicine name:
LongActon 0.07 mg/ml solution for injection for cattle and pigs
Longacton 0.07 mg/ml Oplossing voor injectie
Longacton 0.07 mg/ml Solution injectable
Longacton 0.07 mg/ml Injektionslösung
Active substance:
  • Carbetocin
Target species:
  • Cattle
  • Pig
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Carbetocin
    0.07
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • Intravenous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01BB03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • (ID3) 60 millilitre(s): unspecified outer container with 6 Vial (glass) each with 10 millilitre(s)
  • (ID2) 600 millilitre(s): unspecified outer container with 12 Vial (glass) each with 50 millilitre(s)
  • (ID1) 50 millilitre(s): unspecified outer container with 1 Vial (glass) with 50 millilitre(s)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Vetoquinol
Marketing authorisation date:
Manufacturing sites for batch release:
  • Wirtschaftsgenossenschaft deutscher Tieraerzte e G
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V248981
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0106/001
Concerned member states:
  • Austria
  • Belgium
  • France
  • Ireland
  • Luxembourg
  • Netherlands
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 4/12/2025
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Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/08/2025
Download
French (PDF)
Published on: 18/08/2025
Download
German (PDF)
Published on: 18/08/2025
Download