Calfoset, Injekční roztok
Calfoset, Injekční roztok
Authorised
- Calcium gluconate
- Magnesium chloride hexahydrate
- CALCIUM GLYCEROPHOSPHATE
Product identification
Medicine name:
Calfoset, Injekční roztok
Active substance:
- Calcium gluconate
- Magnesium chloride hexahydrate
- CALCIUM GLYCEROPHOSPHATE
Target species:
-
Horse
-
Cattle
-
Sheep
-
Goat
-
Pig
Route of administration:
-
Intravenous use
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Calcium gluconate328.20milligram(s)1.00millilitre(s)
-
Magnesium chloride hexahydrate41.80milligram(s)1.00millilitre(s)
-
CALCIUM GLYCEROPHOSPHATE81.30milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
- Horse
-
Meat and offal0day
-
- Cattle
-
Meat and offal0day
-
Milk0day
-
- Sheep
-
Meat and offal0day
-
Milk0day
-
- Goat
-
Meat and offal0day
-
Milk0day
-
- Pig
-
Meat and offal0day
-
-
Subcutaneous use
- Horse
-
Meat and offal0day
-
- Cattle
-
Meat and offal0day
-
Milk0day
-
- Sheep
-
Meat and offal0day
-
Milk0day
-
- Goat
-
Meat and offal0day
-
Milk0day
-
- Pig
-
Meat and offal0day
-
-
Intramuscular use
- Horse
-
Meat and offal0day
-
- Cattle
-
Meat and offal0day
-
Milk0day
-
- Sheep
-
Meat and offal0day
-
Milk0day
-
- Goat
-
Meat and offal0day
-
Milk0day
-
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12AX
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- Krka d.d. Novo Mesto
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicines
Authorisation number:
- 96/164/95-C
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.
Czech (PDF)
Published on: 26/10/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
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