Veterinary Medicines Information website

Peni.Strep-Kel Suspensie voor injectie

Authorised
  • Benzylpenicillin procaine
  • Dihydrostreptomycin sulfate
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Product identification

Medicine name:
Peni.Strep-Kel Suspensie voor injectie
Active substance:
  • Benzylpenicillin procaine
  • Dihydrostreptomycin sulfate
Target species:
  • Cattle
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Benzylpenicillin procaine
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Dihydrostreptomycin sulfate
    542.68
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        338
        day
      • Milk
        4
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CE01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • Peni.Strep-Kel Suspension for injection. Box with 12 vials of 250 ml
  • Peni.Strep-Kel Suspension for injection. Box with 12 vials of 100 ml
  • Peni.Strep-Kel Suspension for injection. Box with 12 vials of 50 ml
  • Peni.Strep-Kel Suspension for injection. Box with 12 vials of 30 ml
  • Peni.Strep-Kel Suspension for injection. Box with 1 vial of 30 ml
  • Peni.Strep-Kel Suspension for injection. Box with 1 vial of 50 ml
  • Peni.Strep-Kel Suspension for injection. Box with 1 vial of 100 ml
  • Peni.Strep-Kel Suspension for injection. Box with 1 vial of 250 ml

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:
  • KELA Kempisch Laboratorium Kela Laboratoria
Marketing authorisation date:
Manufacturing sites for batch release:
  • KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V105183
Date of authorisation status change:

Documents

Package Leaflet

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German (PDF)
Published on: 18/08/2025
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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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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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Labelling

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