Veterinary Medicines

Penovet vet. 300.000 a.e./ml stungulyf, dreifa

Authorised
  • Benzylpenicillin procaine
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Product identification

Medicine name:
Penovet vet. 300.000 a.e./ml stungulyf, dreifa
Active substance:
  • Benzylpenicillin procaine
Target species:
  • Cattle
  • Pig
  • Sheep
  • Goat
  • Horse
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Benzylpenicillin procaine
    300.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        3
        day
      • Meat and offal
        15
        day
    • Pig
      • Meat and offal
        5
        day
    • Sheep
      • Meat and offal
        15
        day
    • Goat
      • Meat and offal
        15
        day
      • Milk
        3
        day
    • Horse
      • Meat and offal
        15
        day
  • Subcutaneous use
    • Cattle
      • Milk
        3
        day
      • Meat and offal
        15
        day
    • Pig
      • Meat and offal
        5
        day
    • Sheep
      • Meat and offal
        15
        day
    • Goat
      • Meat and offal
        15
        day
      • Milk
        3
        day
    • Horse
      • Meat and offal
        15
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CE09
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Iceland
Available in:
  • Iceland
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Boehringer Ingelheim Animal Health Denmark A/S
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health Denmark A/S
  • Boehringer Ingelheim Danmark A/S
Responsible authority:
  • Icelandic Medicines Agency
Authorisation number:
  • 960197
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Icelandic (PDF)
Published on: 13/09/2024
Updated on: 25/03/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Icelandic (PDF)
Published on: 13/09/2024
Updated on: 25/03/2025
Download