Veterinary Medicines

LACTOLYTE

Authorised
  • WHEY
  • Sodium acetate
  • Sodium propionate
  • Sodium chloride
  • Potassium chloride
  • Magnesium chloride
  • Potassium dihydrogen phosphate
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Product identification

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

Product details

Active substance and strength:
  • WHEY
    76.88
    gram(s)
    /
    90.00
    gram(s)
  • Sodium acetate
    4.90
    gram(s)
    /
    90.00
    gram(s)
  • Sodium propionate
    1.92
    gram(s)
    /
    90.00
    gram(s)
  • Sodium chloride
    2.92
    gram(s)
    /
    90.00
    gram(s)
  • Potassium chloride
    0.74
    gram(s)
    /
    90.00
    gram(s)
  • Magnesium chloride
    0.38
    gram(s)
    /
    90.00
    gram(s)
  • Potassium dihydrogen phosphate
    1.36
    gram(s)
    /
    90.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water
Withdrawal period by route of administration:
  • Oral use
    • Cattle (calf)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07CQ01
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Luxembourg
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone)
Marketing authorisation holder:
  • Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
  • Virbac
Responsible authority:
  • Ministry Of Health And Social Security
Authorisation number:
  • V/859/92/06/0367
Date of authorisation status change: