Veterinary Medicines

Soludox 500 mg/g powder for use in drinking water for pigs and chickens

Authorised
  • Doxycycline hyclate
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Product identification

Medicine name:
Soludox 500 mg/g powder for use in drinking water for pigs and chickens
Soludox 500 mg/g poeder voor toediening via het drinkwater voor varkens en kippen
Active substance:
  • Doxycycline hyclate
Target species:
  • Chicken
  • Pig
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Doxycycline hyclate
    500.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Oral powder
Withdrawal period by route of administration:
  • Oral use
    • Chicken
      • Meat and offal
        3
        day
      • Meat and offal
        9
        day
    • Pig
      • Meat and offal
        4
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • 500 g pack. The pack consists of the laminate: Polyester - polyethylene - aluminium and an inner layer of ionomer (surlyn).
  • 500 g pack. The pack consists of the laminate: Polyester - polyethylene - aluminium - polyethylene and an inner layer of polyethylene.
  • 500 g pack. The pack consists of the laminate: Polyethylene terephtalic acid - aluminium - polyamide and an inner layer of polyethylene.
  • 250 g pack. The pack consists of the laminate: Polyethylene terephtalic acid - aluminium - polyamide and an inner layer of polyethylene.
  • 250 g pack. The pack consists of the laminate: Polyester - polyethylene - aluminium and an inner layer of ionomer (surlyn).
  • 250 g pack. The pack consists of the laminate: Polyester - polyethylene - aluminium - polyethylene and an inner layer of polyethylene.
  • 10x 100g packs in a carton box. The packs consists of the laminate: Polyethylene terephtalic acid - aluminium - polyamide and an inner layer of polyethylene.
  • 10x 100g packs in a carton box. The packs consists of the laminate: Polyester - polyethylene - aluminium and an inner layer of ionomer (surlyn).
  • 10x 100g packs in a carton box. The packs consists of the laminate: Polyester - polyethylene - aluminium - polyethylene and an inner layer of polyethylene.
  • 100 g pack. The pack consists of the laminate: Polyethylene terephtalic acid - aluminium - polyamide and an inner layer of polyethylene.
  • 100 g pack. The pack consists of the laminate: Polyester - polyethylene - aluminium and an inner layer of ionomer (surlyn).
  • 100 g pack. The pack consists of the laminate: Polyester - polyethylene - aluminium - polyethylene and an inner layer of polyethylene.
  • 1 kg pack. The pack consists of the laminate: Polyethylene terephtalic acid - aluminium - polyamide and an inner layer of polyethylene.
  • 1 kg pack. The pack consists of the laminate: Polyester - polyethylene - aluminium and an inner layer of ionomer (surlyn).
  • 1 kg pack. The pack consists of the laminate: Polyester - polyethylene - aluminium - polyethylene and an inner layer of polyethylene.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Well-established use application (Article 13a 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:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 9612
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0167/001
Concerned member states:
  • Belgium
  • Denmark
  • Hungary
  • Lithuania
  • Poland

Documents

Combined File of all Documents

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Dutch (PDF)
Published on: 28/01/2022
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