Veterinary Medicines

COMBI-kel 40 suspensija injekcijām zirgiem, liellopiem, cūkām, aitām, kazām, suņiem, kaķiem

Authorised
  • Benzylpenicillin procaine
  • Dihydrostreptomycin sulfate
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Product identification

Medicine name:
COMBI-kel 40 suspensija injekcijām zirgiem, liellopiem, cūkām, aitām, kazām, suņiem, kaķiem
Active substance:
  • Benzylpenicillin procaine
  • Dihydrostreptomycin sulfate
Target species:
  • Cattle
  • Goat
  • Sheep
  • Horse
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intraperitoneal use
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Benzylpenicillin procaine
    200000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • Dihydrostreptomycin sulfate
    200000.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intraperitoneal use
    • Cattle
      • Meat and offal
        30
        day
      • Milk
        4
        day
    • Goat
      • Milk
        4
        day
      • Meat and offal
        30
        day
    • Sheep
      • Milk
        4
        day
      • Meat and offal
        30
        day
    • Horse
      • Milk
        no withdrawal period
  • Intramuscular use
    • Cattle
      • Meat and offal
        30
        day
      • Milk
        4
        day
    • Sheep
      • Meat and offal
        30
        day
      • Milk
        4
        day
    • Goat
      • Meat and offal
        30
        day
      • Milk
        4
        day
    • Horse
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        30
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01RA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Latvia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • KELA Kempisch Laboratorium Kela Laboratoria
Marketing authorisation date:
Manufacturing sites for batch release:
  • KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
  • Food And Veterinary Service
Authorisation number:
  • V/NRP/98/0716
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.
Latvian (PDF)
Published on: 9/02/2026
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Package Leaflet

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Latvian (PDF)
Published on: 9/02/2026
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 9/02/2026
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