CALIERCORTIN 4 mg/ml solution for injection for cattle, pigs, horses, dogs and cats
CALIERCORTIN 4 mg/ml solution for injection for cattle, pigs, horses, dogs and cats
Authorised
- Dexamethasone sodium phosphate
Product identification
Medicine name:
CALIERCORTIN 4 mg/ml ενέσιμο διάλυμα για άλογα, βοοειδή, χοίρους, σκύλους και γάτες
CALIERCORTIN 4 mg/ml solution for injection for cattle, pigs, horses, dogs and cats
Active substance:
- Dexamethasone sodium phosphate
Target species:
-
Cattle
-
Dog
-
Horse
-
Cat
-
Pig
Route of administration:
-
Intravenous use
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Dexamethasone sodium phosphate5.30milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Milk4day
-
Meat and offal16day
-
-
Dog
-
Horse
-
Meat and offal16day
-
Milkno withdrawal periodNot authorised for use in mares producing milk for human consumption.
-
-
Cat
-
Pig
-
Meat and offal4day
-
-
-
Subcutaneous use
-
Cattle
-
Milk4day
-
Meat and offal16day
-
-
Dog
-
Horse
-
Meat and offal16day
-
Milkno withdrawal periodNot authorised for use in mares producing milk for human consumption.
-
-
Cat
-
Pig
-
Meat and offal4day
-
-
-
Intramuscular use
-
Cattle
-
Milk4day
-
Meat and offal16day
-
-
Dog
-
Horse
-
Meat and offal16day
-
Milkno withdrawal periodNot authorised for use in mares producing milk for human consumption.
-
-
Cat
-
Pig
-
Meat and offal4day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH02AB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Cyprus
Available in:
-
Cyprus
Package description:
- (ID2): 1 unspecified outer container with 1 Vial (Glass) with 50 millilitre(s) (50 millilitre(s))
- (ID1): 1 unspecified outer container with 1 Vial (Glass) with 10 millilitre(s) (10 millilitre(s))
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Laboratorios Calier S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Calier S.A.
Responsible authority:
- Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
- CY00713V
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0179/001
Concerned member states:
-
Austria
-
Bulgaria
-
Croatia
-
Cyprus
-
Greece
-
Italy
-
Poland
-
Portugal
-
Romania
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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in another language below.
Greek (PDF)
Published on: 8/12/2022
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