GLUCALENE, soluzione iniettabile per bovini, suini, equini
GLUCALENE, soluzione iniettabile per bovini, suini, equini
Authorised
- Calcium gluconate
- Magnesium gluconate
- Phosphorylcolamine
- Cyanocobalamin
Product identification
Medicine name:
GLUCALENE, soluzione iniettabile per bovini, suini, equini
Active substance:
- Calcium gluconate
- Magnesium gluconate
- Phosphorylcolamine
- Cyanocobalamin
Target species:
-
Cattle
-
Pig
-
Horse
Route of administration:
-
Subcutaneous use
-
Intravenous use
-
Intraperitoneal use
-
Intramuscular use
Product details
Active substance and strength:
-
Calcium gluconate20.00gram(s)100.00millilitre(s)
-
Magnesium gluconate5.00gram(s)100.00millilitre(s)
-
Phosphorylcolamine5.00gram(s)100.00millilitre(s)
-
Cyanocobalamin3.00milligram(s)100.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Milk0day
-
Meat and offal0day
-
- Pig
-
Meat and offal0day
-
- Horse
-
Milk0day
-
Meat and offal0day
-
-
Intravenous use
- Horse
-
Milk0day
-
Meat and offal0day
-
- Pig
-
Meat and offal0day
-
- Cattle
-
Milk0day
-
Meat and offal0day
-
-
Intraperitoneal use
- Cattle
-
Milk0day
-
Meat and offal0day
-
- Pig
-
Meat and offal0day
-
- Horse
-
Milk0day
-
Meat and offal0day
-
-
Intramuscular use
- Cattle
-
Milk0day
-
Meat and offal0day
-
- Pig
-
Meat and offal0day
-
- Horse
-
Milk0day
-
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:
-
Italy
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:
- Ceva Salute Animale S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
- Vetem S.p.A.
Responsible authority:
- Ministry Of Health
Authorisation number:
- 1015340
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Italian (PDF)
Published on: 7/06/2023
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