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Veterinary Medicines

Octacillin, 800 mg/g powder for oral solution for chickens

Authorised
  • Amoxicillin trihydrate

Product identification

Medicine name:
Octacillin, 800 mg/g powder for oral solution for chickens
Octacillin 800 mg/g poeder voor gebruik in het drinkwater voor kippen
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Chicken
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Amoxicillin trihydrate
    800.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • Chicken
      • Meat and offal
        1
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • Sachet 500 g. Sachets consist of a polyester layer on the outside, inside layers of aluminium and polyamide and an inner layer of polyethylene.
  • Sachet 250 g. Sachets consist of a white layer on the outside, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
  • Sachet 500 g. Sachets consist of a white layer on the outside, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
  • Sachet 250 g. Sachets consist of a polyester layer on the outside, inside layers of aluminium and polyamide and an inner layer of polyethylene.
  • Sachet 100 g. Sachets consist of a white layer on the outside, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
  • Sachet 100 g. Sachets consist of a polyester layer on the outside, inside layers of aluminium and polyamide and an inner layer of polyethylene.
  • Sachet 1.0 kg. Sachets consist of a white layer on the outside, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
  • Sachet 1.0 kg. Sachets consist of a polyester layer on the outside, inside layers of aluminium and polyamide and an inner layer of polyethylene.

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Eurovet Animal Health B.V.
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 104691
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0144/001
Concerned member states:
  • France
  • Germany

Documents

Combined File of all Documents

English (PDF)
Published on: 13/06/2022
Download
Dutch (PDF)
Published on: 29/01/2022

octacilin par.pdf

Dutch (PDF)
Published on: 13/06/2022
Download
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