LODEVIL
LODEVIL
Authorised
- Glucose
- Magnesium chloride
- Potassium chloride
- Sodium chloride
- Sodium hydrogen carbonate
- Sodium acetate
Product identification
Medicine name:
LODEVIL
Active substance:
- Glucose
- Magnesium chloride
- Potassium chloride
- Sodium chloride
- Sodium hydrogen carbonate
- Sodium acetate
Target species:
-
Cattle (calf)
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
Glucose10.80milligram(s)1.00millilitre(s)
-
Magnesium chloride0.20milligram(s)1.00millilitre(s)
-
Potassium chloride0.45milligram(s)1.00millilitre(s)
-
Sodium chloride3.51milligram(s)1.00millilitre(s)
-
Sodium hydrogen carbonate4.20milligram(s)1.00millilitre(s)
-
Sodium acetate4.08milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for infusion
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle (calf)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QB05BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- Available only in French
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetoquinol S.A.
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/3830006 4/1982
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
How useful was this page?: