LACTOLYTE
LACTOLYTE
Authorised
- WHEY
- POTASSIUM PHOSPHATE
- Magnesium chloride
- Potassium chloride
- Sodium chloride
- Sodium propionate
- Sodium acetate
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:
-
WHEY854.20milligram(s)1.00gram(s)
-
POTASSIUM PHOSPHATE15.11milligram(s)1.00gram(s)
-
Magnesium chloride4.22milligram(s)1.00gram(s)
-
Potassium chloride8.22milligram(s)1.00gram(s)
-
Sodium chloride32.44milligram(s)1.00gram(s)
-
Sodium propionate21.33milligram(s)1.00gram(s)
-
Sodium acetate54.50milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Cattle (calf)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07CQ02
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
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:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 4/04/2022
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