TAT CALCI 50, Solução Injetável para bovinos, equinos, suínos, ovinos e caprinos e cães
TAT CALCI 50, Solução Injetável para bovinos, equinos, suínos, ovinos e caprinos e cães
Authorised
- Magnesium chloride
- Calcium hydroxide
- Calcium borogluconate
- Calcium gluconate monohydrate
Product identification
Medicine name:
TAT CALCI 50, Solução Injetável para bovinos, equinos, suínos, ovinos e caprinos e cães
Active substance:
- Magnesium chloride
- Calcium hydroxide
- Calcium borogluconate
- Calcium gluconate monohydrate
Target species:
-
Dog
-
Cattle
-
Horse
-
Pig
-
Sheep
-
Goat
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Magnesium chloride6.50/gram(s)100.00millilitre(s)
-
Calcium hydroxide1.32/gram(s)100.00millilitre(s)
-
Calcium borogluconate42.90/gram(s)100.00millilitre(s)
-
Calcium gluconate monohydrate3.10/gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Horse
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Meat and offal0day
-
Milk0day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12AA20
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Available in:
-
Portugal
Package description:
- Available only in Portuguese
- Available only in Portuguese
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:
- aniMedica GmbH
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 740/01/13NFVPT
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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Portuguese (PDF)
Published on: 10/02/2026