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Octacillin, 800 mg/g powder for oral solution for chickens
  • Amoxicillin trihydrate
  • Valid

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 and strength:
  • Amoxicillin trihydrate
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Authorisation number:
  • REG NL 104691
Product identification number:
  • 37e2ca96-27a4-4308-ae42-3a6301dfb524
Permanent identification number:
  • 600000037122

Product details

Pharmaceutical form:
  • Powder for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • Chicken
      • Meat and offal
        1
        day

Availability

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.
Manufacturing sites for batch release:
  • Eurovet Animal Health B.V.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
  • NL/V/0144/001
Date of authorisation status change:
Authorisation country:
  • Netherlands
Responsible authority:
  • Medicines Evaluation Board
Marketing authorisation holder:
  • Eurovet Animal Health B.V.
Marketing authorisation issued:
Reference member state:
  • Netherlands
Concerned member states:
  • France
  • Germany
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

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