Dexadreson 2 mg/ml injekčný roztok pre hovädzí dobytok, kone, ošípané, psy a mačky
Dexadreson 2 mg/ml injekčný roztok pre hovädzí dobytok, kone, ošípané, psy a mačky
Authorised
- Dexamethasone sodium phosphate
Product identification
Medicine name:
Dexadreson 2 mg/ml injekčný roztok pre hovädzí dobytok, kone, ošípané, psy a mačky
Active substance:
- Dexamethasone sodium phosphate
Target species:
-
Cattle
-
Pig
-
Dog
-
Cat
-
Horse
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Intraarticular use
Product details
Active substance and strength:
-
Dexamethasone sodium phosphate2.63/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal8day
-
Milk72hour
-
-
Pig
-
Meat and offal2day
-
-
-
Intravenous use
-
Horse
-
Meat and offal8dayDo not administer to mares whose milk is intended for human consumption.
-
-
-
Intraarticular use
-
Horse
-
Meat and offal8dayDo not administer to mares whose milk is intended for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH02AB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Available in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International GmbH
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/049/07-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 4/08/2025