Veterinary Medicines

Lactolyte

Not authorised
  • Magnesium chloride
  • Potassium chloride
  • Potassium dihydrogen phosphate
  • Sodium chloride
  • Sodium acetate
  • Sodium propionate
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Product identification

Medicine name:
Lactolyte
Active substance:
  • Magnesium chloride
  • Potassium chloride
  • Potassium dihydrogen phosphate
  • Sodium chloride
  • Sodium acetate
  • Sodium propionate
Target species:
  • Cattle (calf)
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Magnesium chloride
    4.20
    milligram(s)
    /
    1.00
    gram(s)
  • Potassium chloride
    8.20
    milligram(s)
    /
    1.00
    gram(s)
  • Potassium dihydrogen phosphate
    15.10
    milligram(s)
    /
    1.00
    gram(s)
  • Sodium chloride
    32.40
    milligram(s)
    /
    1.00
    gram(s)
  • Sodium acetate
    54.40
    milligram(s)
    /
    1.00
    gram(s)
  • Sodium propionate
    21.30
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Oral powder
Withdrawal period by route of administration:
  • Oral use
    • Cattle (calf)
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07CQ01
Legal status of supply:
  • Medicinal product not subject to medical prescription
Authorisation status:
  • Surrendered
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:
  • Virbac Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Virbac
Responsible authority:
  • MEB
Authorisation number:
  • REG NL 2393
Date of authorisation status change:

Documents

Combined File of all Documents

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Dutch (PDF)
Published on: 22/02/2022
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