Calcitat forte - Injektionslösung für Tiere
Calcitat forte - Injektionslösung für Tiere
Authorised
- Calcium gluconate monohydrate
- Calcium oxide
- Magnesium chloride hexahydrate
- Phosphorylcolamine
Product identification
Medicine name:
Calcitat forte - Injektionslösung für Tiere
Active substance:
- Calcium gluconate monohydrate
- Calcium oxide
- Magnesium chloride hexahydrate
- Phosphorylcolamine
Target species:
-
Cattle
-
Dog
-
Goat
-
Sheep
-
Cat
-
Pig
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Calcium gluconate monohydrate430.00milligram(s)1.00millilitre(s)
-
Calcium oxide10.00milligram(s)1.00millilitre(s)
-
Magnesium chloride hexahydrate65.00milligram(s)1.00millilitre(s)
-
Phosphorylcolamine6.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal0day
-
Milk0hour
-
- Dog
- Goat
-
Meat and offal0day
-
Milk0hour
-
- Sheep
-
Meat and offal0day
-
Milk0hour
-
- Cat
- Pig
-
Meat and offal0day
-
-
Intravenous use
- Cattle
-
Meat and offal0day
-
Milk0hour
-
- Dog
- Goat
-
Meat and offal0day
-
Milk0hour
-
- Sheep
-
Meat and offal0day
-
Milk0hour
-
- Cat
- Pig
-
Meat and offal0day
-
-
Subcutaneous use
- Cattle
-
Meat and offal0day
-
Milk0hour
-
- Dog
- Goat
-
Meat and offal0day
-
Milk0hour
-
- Sheep
-
Meat and offal0day
-
Milk0hour
-
- Cat
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12AA20
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Animedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Pasteur Filiala Filipesti S.A.
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 8-00021
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 21/11/2023
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 19/04/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 19/04/2022
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