CALCITAT FORT SOLUTION INJECTABLE
CALCITAT FORT SOLUTION INJECTABLE
Authorised
- Calcium gluconate monohydrate
- Phosphorylcolamine
- Magnesium chloride hexahydrate
Product identification
Medicine name:
CALCITAT FORT SOLUTION INJECTABLE
Active substance:
- Calcium gluconate monohydrate
- Phosphorylcolamine
- Magnesium chloride hexahydrate
Target species:
-
Cattle
-
Pig
-
Horse
-
Horse (mare)
-
Sheep
-
Goat
-
Dog
Route of administration:
-
Intramuscular use
-
Subcutaneous use
-
Intravenous use
Product details
Active substance and strength:
-
Calcium gluconate monohydrate430.00/milligram(s)1.00millilitre(s)
-
Phosphorylcolamine6.00/milligram(s)1.00millilitre(s)
-
Magnesium chloride hexahydrate65.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
Horse (mare)
-
Milk0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Meat and offal0day
-
Milk0day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
Horse (mare)
-
Milk0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Meat and offal0day
-
Milk0day
-
-
-
Intravenous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
Horse (mare)
-
Milk0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12AX
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Available 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:
- Intervet
Marketing authorisation date:
Manufacturing sites for batch release:
- Lohmann Animal Health GmbH & Co. KG
- Trirx Segre
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/5167900 6/1992
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: 4/07/2025
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 4/07/2025