Kaltetan, 250 mg/ml + 80 mg/ml + 10 mg/ml solution for infusion for horses, cattle and pigs
Kaltetan, 250 mg/ml + 80 mg/ml + 10 mg/ml solution for infusion for horses, cattle and pigs
Authorised
- CALCIUM GLUCONATE FOR INJECTION
- Magnesium chloride hexahydrate
- Sodium glycerophosphate pentahydrate
Product identification
Medicine name:
Kaltetan, 250 mg/ml + 80 mg/ml + 10 mg/ml solution for infusion for horses, cattle and pigs
Kaltetan, 250 mg/ml + 80 mg/ml + 10 mg/ml soluzione per infusione per cavalli, bovini e suini
Active substance:
- CALCIUM GLUCONATE FOR INJECTION
- Magnesium chloride hexahydrate
- Sodium glycerophosphate pentahydrate
Target species:
-
Horse
-
Pig
-
Cattle
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
CALCIUM GLUCONATE FOR INJECTION250.00milligram(s)/millilitre1.00milligram(s)/millilitre
-
Magnesium chloride hexahydrate80.00milligram(s)1.00millilitre(s)
-
Sodium glycerophosphate pentahydrate10.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for infusion
Withdrawal period by route of administration:
-
Intravenous use
- Horse
-
Milk5weekMeat and offal: Zero days. Milk: Zero hours
-
- Pig
-
Meat and offal5weekMeat and offal: Zero days
-
- Cattle
-
Milk5weekMeat and offal: Zero days. Milk: Zero hours
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12AX
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Available in:
-
Italy
Package description:
- Polypropylene (PP) bottles closed with a bromobutyl rubber stopper, type I and secured with an aluminium cap. Package size: 500 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Vet-Agro Multi-Trade Company Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Multi-Trade Company "Vet-Agro" Sp. z o.o.
Responsible authority:
- Ministry Of Health
Authorisation number:
- 105612
Date of authorisation status change:
Reference member state:
-
Poland
Procedure number:
- PL/V/0110/001
Concerned member states:
-
Bulgaria
-
Czechia
-
Greece
-
Hungary
-
Italy
-
Lithuania
-
Portugal
-
Romania
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 19/08/2022
How useful was this page?: