Calcitat S 50
Calcitat S 50
Authorised
- CALCIUM GLUCONATE FOR INJECTION
- Magnesium chloride hexahydrate
- Phosphorylcolamine
- Calcium hydroxide
- Calcium borogluconate
Product identification
Medicine name:
Calcitat S 50
Active substance:
- CALCIUM GLUCONATE FOR INJECTION
- Magnesium chloride hexahydrate
- Phosphorylcolamine
- Calcium hydroxide
- Calcium borogluconate
Target species:
-
Cattle
-
Cattle (calf)
-
Dog
-
Goat
-
Sheep
-
Cat
-
Pig
-
Pig (piglet)
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
CALCIUM GLUCONATE FOR INJECTION3.10gram(s)100.00millilitre(s)
-
Magnesium chloride hexahydrate6.50gram(s)100.00millilitre(s)
-
Phosphorylcolamine0.60gram(s)100.00millilitre(s)
-
Calcium hydroxide1.32gram(s)100.00millilitre(s)
-
Calcium borogluconate42.90gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal0day
-
-
Cattle (calf)
-
Meat and offal0day
-
-
Dog
-
Goat
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
Cat
-
Pig
-
Meat and offal0day
-
-
Pig (piglet)
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal0day
-
-
Cattle (calf)
-
Meat and offal0day
-
-
Dog
-
Goat
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
Cat
-
Pig
-
Meat and offal0day
-
-
Pig (piglet)
-
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:
-
Germany
Available in:
-
Germany
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:
- aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Pasteur Filiala Filipesti S.A.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 1468.01.01
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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in another language below.
German (PDF)
Published on: 2/09/2024
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