Veterinary Medicines

Biopect, poeder voor gebruik in drinkwater/melk voor kalveren, lammeren en biggen

Authorised
  • Sodium hydrogen carbonate
  • Ascorbic acid
  • Potassium dihydrogen phosphate
  • Sodium chloride
  • Citric acid
  • Glucose monohydrate
  • Magnesium chloride
  • Potassium chloride
  • Magnesium oxide
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Product identification

Medicine name:
Biopect, poeder voor gebruik in drinkwater/melk voor kalveren, lammeren en biggen
Active substance:
  • Sodium hydrogen carbonate
  • Ascorbic acid
  • Potassium dihydrogen phosphate
  • Sodium chloride
  • Citric acid
  • Glucose monohydrate
  • Magnesium chloride
  • Potassium chloride
  • Magnesium oxide
Target species:
  • Cattle (calf)
  • Sheep (lamb)
  • Pig (piglet)
Route of administration:
  • In drinking water/milk use

Product details

Active substance and strength:
  • Sodium hydrogen carbonate
    36.80
    milligram(s)
    /
    1.00
    gram(s)
  • Ascorbic acid
    4.40
    milligram(s)
    /
    1.00
    gram(s)
  • Potassium dihydrogen phosphate
    5.30
    milligram(s)
    /
    1.00
    gram(s)
  • Sodium chloride
    38.50
    milligram(s)
    /
    1.00
    gram(s)
  • Citric acid
    13.10
    milligram(s)
    /
    1.00
    gram(s)
  • Glucose monohydrate
    301.00
    milligram(s)
    /
    1.00
    gram(s)
  • Magnesium chloride
    0.90
    milligram(s)
    /
    1.00
    gram(s)
  • Potassium chloride
    12.30
    milligram(s)
    /
    1.00
    gram(s)
  • Magnesium oxide
    1.80
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water/milk
Withdrawal period by route of administration:
  • In drinking water/milk use
    • Cattle (calf)
      • Meat and offal
        no withdrawal period
    • Sheep (lamb)
      • Meat and offal
        no withdrawal period
    • Pig (piglet)
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07CQ02
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Vee-Service Drunen B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Biofiber-Damino A/S
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 5010
Date of authorisation status change:

Documents

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Published on: 22/02/2022
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