Calcitat 50, solution for infusion and injection in cattle
Calcitat 50, solution for infusion and injection in cattle
Authorised
- Calcium gluconate monohydrate
- Calcium borogluconate
- Calcium hydroxide
- Magnesium chloride hexahydrate
Product identification
Medicine name:
Calcitat 50, solution for infusion and injection in cattle
Active substance:
- Calcium gluconate monohydrate
- Calcium borogluconate
- Calcium hydroxide
- Magnesium chloride hexahydrate
Target species:
-
Cattle
Route of administration:
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Calcium gluconate monohydrate3.10/gram(s)100.00millilitre(s)
-
Calcium borogluconate42.90/gram(s)100.00millilitre(s)
-
Calcium hydroxide1.32/gram(s)100.00millilitre(s)
-
Magnesium chloride hexahydrate6.50/gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Solution for injection/infusion
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12AA
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- 1 500 ml bottle.Vial: 500 ml sterile plastic bottle (Type PP28).Stopper: Chlorobutyl rubber stopper.Cap: Aluminium cap.
- 1 250 ml bottle.Vial: 250 ml sterile plastic bottle (Type PP28).Stopper: Chlorobutyl rubber stopper.Cap: Aluminium cap.
- 1 100 ml bottleVial: 100 ml HK2 colourless glass bottle.Stopper: Bromobutyl rubber stopper.Cap: Aluminium cap.
- 60 250 ml bottles.Vial: 250 ml sterile plastic bottle (Type PP28).Stopper: Chlorobutyl rubber stopper.Cap: Aluminium cap.
- 12 100 ml bottles.Vial: 100 ml HK2 colourless glass bottle.Stopper: Bromobutyl rubber stopper.Cap: Aluminium cap.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
- aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Pasteur Filiala Filipesti S.A.
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10826/001/002
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
English (PDF)
Download Published on: 3/05/2024
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