Veterinary Medicine Information website

Ampiclox Quick Release 75 mg/3 g - 200 mg/3 g Suspensie voor intramammair gebruik

Authorised
  • Cloxacillin sodium
  • Ampicillin sodium
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Product identification

Medicine name:
Ampiclox Quick Release 75 mg/3 g - 200 mg/3 g Suspensie voor intramammair gebruik
Active substance:
  • Cloxacillin sodium
  • Ampicillin sodium
Target species:
  • Cattle (lactating cow)
Route of administration:
  • Intramammary use

Product details

Active substance and strength:
  • Cloxacillin sodium
    218.40
    milligram(s)
    /
    1.00
    Syringe
  • Ampicillin sodium
    79.70
    milligram(s)
    /
    1.00
    Syringe
Pharmaceutical form:
  • Intramammary suspension
Withdrawal period by route of administration:
  • Intramammary use
    • Cattle (lactating cow)
      • Meat and offal
        2
        day
      • Milk
        60
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ51CF02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • Ampiclox Quick Release 30 3 g Syringe Intramammary suspension
  • Ampiclox Quick Release 24 3 g Tube Intramammary suspension
  • Ampiclox Quick Release 12 3 g Syringe Intramammary suspension
  • Ampiclox Quick Release 3 3 g Syringe Intramammary suspension

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:
  • Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
  • Haupt Pharma Latina S.r.l.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V095645
Date of authorisation status change:

Documents

Summary of Product Characteristics

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French (PDF)
Published on: 18/08/2025
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Dutch (PDF)
Published on: 18/08/2025
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Package Leaflet

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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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Dutch (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.
French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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Dutch (PDF)
Published on: 18/08/2025
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