Veterinary Medicines

ILCOCILLIN P.S. (200.000IU+250MG)/ML ΕΝΕΣΙΜΟ ΕΝΑΙΩΡΗΜΑ

Authorised
  • Benzylpenicillin procaine monohydrate
  • Dihydrostreptomycin sulfate
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Product identification

Medicine name:
ILCOCILLIN P.S. (200.000IU+250MG)/ML ΕΝΕΣΙΜΟ ΕΝΑΙΩΡΗΜΑ
Active substance:
  • Benzylpenicillin procaine monohydrate
  • Dihydrostreptomycin sulfate
Target species:
  • Cattle
  • Sheep (for meat production)
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Benzylpenicillin procaine monohydrate
    200000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • Dihydrostreptomycin sulfate
    250.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        28
        day
      • Milk
        6
        day
      • Milk
        8
        day
    • Sheep (for meat production)
      • Meat and offal
        28
        day
    • Pig
      • Meat and offal
        28
        day
    • Dog
      • Not applicable
        no withdrawal period
    • Cat
      • Not applicable
        no withdrawal period
  • Subcutaneous use
    • Cattle
    • Sheep (for meat production)
    • Pig
    • Dog
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01RA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Greece
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone)
Marketing authorisation holder:
  • Premier Shukuroglou Hellas S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories (Ireland) Limited
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 26783/08-04-2013/K-0045401
Date of authorisation status change:
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