Veterinary Medicine Information website

LACTOLYTE

Not authorised
  • WHEY
  • POTASSIUM PHOSPHATE
  • Magnesium chloride
  • Potassium chloride
  • Sodium chloride
  • Sodium propionate
  • Sodium acetate
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Product identification

Medicine name:
LACTOLYTE
Active substance:
  • WHEY
  • POTASSIUM PHOSPHATE
  • Magnesium chloride
  • Potassium chloride
  • Sodium chloride
  • Sodium propionate
  • Sodium acetate
Target species:
  • Cattle (calf)
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • WHEY
    854.20
    milligram(s)
    /
    1.00
    gram(s)
  • POTASSIUM PHOSPHATE
    15.11
    milligram(s)
    /
    1.00
    gram(s)
  • Magnesium chloride
    4.22
    milligram(s)
    /
    1.00
    gram(s)
  • Potassium chloride
    8.22
    milligram(s)
    /
    1.00
    gram(s)
  • Sodium chloride
    32.44
    milligram(s)
    /
    1.00
    gram(s)
  • Sodium propionate
    21.33
    milligram(s)
    /
    1.00
    gram(s)
  • Sodium acetate
    54.50
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Cattle (calf)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07CQ02
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • France
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
Marketing authorisation date:
Manufacturing sites for batch release:
  • Virbac
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/5676564 5/1984
Date of authorisation status change:

Documents

Summary of Product Characteristics

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French (PDF)
Published on: 4/04/2022
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