Kaltetan forte, 458.4 mg/ml + 125 mg/ml + 20 mg/ml solution for infusion for horses, cattle and pigs
Kaltetan forte, 458.4 mg/ml + 125 mg/ml + 20 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 forte, 458.4 mg/ml + 125 mg/ml + 20 mg/ml solution for infusion for horses, cattle and pigs
Калтетан форте, 458,4 mg/ml + 125 mg/ml + 20 mg/ml инфузионен разтвор за коне
Active substance:
- CALCIUM GLUCONATE FOR INJECTION
- Magnesium chloride hexahydrate
- Sodium glycerophosphate pentahydrate
Target species:
-
Horse
-
Cattle
-
Pig
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
CALCIUM GLUCONATE FOR INJECTION458.40milligram(s)1.00millilitre(s)
-
Magnesium chloride hexahydrate125.00milligram(s)1.00millilitre(s)
-
Sodium glycerophosphate pentahydrate20.00milligram(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
-
- Cattle
-
Meat and offal5weekMeat and offal: Zero days. Milk: Zero hours
-
- Pig
-
Meat and offal5weekMeat and offal: Zero days
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12AX
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Available in:
-
Bulgaria
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:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-3110
Date of authorisation status change:
Reference member state:
-
Poland
Procedure number:
- PL/V/0110/002
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
Summary of Product Characteristics
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Bulgarian (PDF)
Published on: 21/07/2022
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