Veterinary Medicines Information website

Pen & Strep Suspension for Injection

Authorised
  • Benzylpenicillin procaine
  • Dihydrostreptomycin sulfate
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Product identification

Medicine name:
Pen & Strep Suspension for Injection
Active substance:
  • Benzylpenicillin procaine
  • Dihydrostreptomycin sulfate
Target species:
  • Cattle
  • Sheep
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Benzylpenicillin procaine
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Dihydrostreptomycin sulfate
    292.02
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        21
        day
      • Milk
        48
        hour
    • Sheep
      • Meat and offal
        28
        day
      • Milk
        48
        hour
    • Pig
      • Meat and offal
        18
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01RA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • Multidose 50 ml uncoloured Type II (Ph. Eur.) plastic (PET) vial sealed with a bromobutyl rubber stopper and aluminium cap, containing a white to off-white sterile suspension.
  • Multidose 100 ml uncoloured Type II (Ph. Eur.) plastic (PET) vial sealed with a bromobutyl rubber stopper and aluminium cap, containing a white to off-white sterile suspension.
  • 250 ml plastic (PET) vials sealed with a bromobutyl rubber stopper andaluminium cap, containing a white to off-white sterile suspension.
  • Multidose 100 ml uncoloured Type II (Ph. Eur.) glass vial sealed with a bromobutyl rubber stopper and aluminium cap, containing a white to off-white sterile suspension.
  • Multidose 50 ml uncoloured Type II (Ph. Eur.) glass vial sealed with a bromobutyl rubber stopper and aluminium cap, containing a white to off-white sterile suspension.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Norbrook Manufacturing Limited
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA22664/009/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 16/01/2026
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