Veterinary Medicine Information website

Bicormicina L.A.

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

Medicine name:
Bicormicina L.A.
Active substance:
  • Benzylpenicillin procaine
  • Benzathine benzylpenicillin
  • Dihydrostreptomycin sulfate
  • Dexamethasone sodium phosphate
  • Dexamethasone isonicotinate
Target species:
  • Cattle
  • Pig
  • Horse
  • Dog
  • Cat
  • Goat
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
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Dexamethasone isonicotinate
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        60
        day
      • Milk
        14
        day
    • Pig
      • Meat and offal
        60
        day
    • Horse
      • Meat and offal
        60
        day
    • Goat
      • Meat and offal
        60
        day
      • Milk
        14
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01RA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Suspended
Authorised in:
  • Italy
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Fatro S.p.A.
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 101708
Date of authorisation status change: