Veterinary Medicines

Bicormicina L.A. suspensija injekcijām liellopiem, sporta zirgiem, kazām, cūkām, suņiem un kaķiem

Authorised
  • Benzylpenicillin procaine
  • Benzathine benzylpenicillin
  • Dihydrostreptomycin sulfate
  • Dexamethasone sodium phosphate
  • Dexamethasone isonicotinate
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Product identification

Medicine name:
Bicormicina L.A. suspensija injekcijām liellopiem, sporta zirgiem, kazām, cūkām, suņiem un kaķiem
Active substance:
  • Benzylpenicillin procaine
  • Benzathine benzylpenicillin
  • Dihydrostreptomycin sulfate
  • Dexamethasone sodium phosphate
  • Dexamethasone isonicotinate
Target species:
  • Cattle
  • Horse (non food-producing)
  • Goat
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Benzylpenicillin procaine
    125000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • Benzathine benzylpenicillin
    125000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • Dihydrostreptomycin sulfate
    250.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Dexamethasone sodium phosphate
    0.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • Dexamethasone isonicotinate
    0.20
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        60
        day
      • Milk
        14
        day
    • Horse (non food-producing)
    • Goat
      • Meat and offal
        60
        day
      • Milk
        14
        day
    • Pig
      • Meat and offal
        60
        day
    • Dog
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01RV01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Latvia
Available 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:
  • Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Fatro S.p.A.
Responsible authority:
  • Food And Veterinary Service
Authorisation number:
  • V/NRP/02/1495
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: 7/06/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 7/06/2024
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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: 7/06/2024
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