Veterinary Medicines

Octacillin 800 mg/g powder for use in drinking water for pigs, amoxicillin trihydrate

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
Octacillin 800 mg/g powder for use in drinking water for pigs, amoxicillin trihydrate
Octacillin Vet. 800 mg/g pulver til anvendelse i drikkevand
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Pig
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
    • Pig
      • Meat and offal
        2
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Denmark
Package description:
  • 500 g multilayer sachet consisting of the following materials: on the outside a white layer, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene
  • 250 g multilayer sachet consisting of the following materials: on the outside a white layer, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene
  • 100 g multilayer sachet consisting of the following materials: on the outside a white layer, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene
  • 1 kg multilayer sachet consisting of the following materials: on the outside a polyester layer, inside layers of aluminium and polyamide and an inner layer of polyethylene
  • 250 g multilayer sachet consisting of the following materials: on the outside a polyester layer, inside layers of aluminium and polyamide and an inner layer of polyethylene
  • 500 g multilayer sachet consisting of the following materials: on the outside a polyester layer, inside layers of aluminium and polyamide and an inner layer of polyethylene
  • 100 g multilayer sachet consisting of the following materials: on the outside a polyester layer, inside layers of aluminium and polyamide and an inner layer of polyethylene
  • 1 kg multilayer sachet consisting of the following materials: on the outside a white layer, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Eurovet Animal Health B.V.
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 37504
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0367/001
Concerned member states:
  • Austria
  • Belgium
  • Croatia
  • Czechia
  • Denmark
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Danish (, PULVER TIL ANVENDELSE I DRIKKEVAND 800 MG-G)
Published on: 29/06/2023
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