Calcibel Forte, 380/60/50mg/ml, Solution for infusion
Calcibel Forte, 380/60/50mg/ml, Solution for infusion
Authorised
- Calcium gluconate
- Magnesium chloride hexahydrate
- Boric acid
Product identification
Medicine name:
Calcibel Forte, 380/60/50mg/ml, Solution for infusion
CALCIBEL FORTE (380+60+50)MG/ML ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ ΓΙΑ ΕΝΔΟΦΛΕΒΙΑ ΕΓΧΥΣΗ
Active substance:
- Calcium gluconate
- Magnesium chloride hexahydrate
- Boric acid
Target species:
-
Horse
-
Cattle
-
Sheep
-
Goat
-
Pig
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
Calcium gluconate380.00milligram(s)1.00millilitre(s)
-
Magnesium chloride hexahydrate60.00milligram(s)1.00millilitre(s)
-
Boric acid50.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for infusion
Withdrawal period by route of administration:
-
Intravenous use
-
Horse
-
Milk0hour
-
Meat and offal0day
-
-
Cattle
-
Milk0hour
-
Meat and offal0day
-
-
Sheep
-
Milk0hour
-
Meat and offal0day
-
-
Goat
-
Milk0hour
-
Meat and offal0day
-
-
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:
-
Greece
Available in:
-
Greece
Package description:
- Plastic Bottle 12 x 500.0 millilitre(s)
- Plastic Bottle 1 x 500.0 millilitre(s)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Bela-Pharm GmbH & Co. KG
Marketing authorisation date:
Manufacturing sites for batch release:
- Bela-Pharm GmbH & Co. KG
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 84808/21-09-2021/K-0214302
Date of authorisation status change:
Reference member state:
-
Czechia
Procedure number:
- CZ/V/0170/001
Concerned member states:
-
Austria
-
Cyprus
-
Denmark
-
Estonia
-
Finland
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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