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VETRIMOXIN 500 mg/g prášok na perorálny roztok

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
VETRIMOXIN 500 mg/g prášok na perorálny roztok
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Pig
  • Chicken (broiler)
  • Cattle (pre-ruminant)
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Amoxicillin trihydrate
    500.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for oral solution
Withdrawal period by route of administration:
  • In drinking water use
    • Pig
      • Meat and offal
        7
        day
    • Chicken (broiler)
      • Meat and offal
        3
        day
    • Cattle (pre-ruminant)
      • Meat and offal
        1
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Ceva Animal Health Slovakia s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Sante Animale
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/109/04-S
Date of authorisation status change:

Documents

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Published on: 6/12/2021
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