DEXACORTYL
DEXACORTYL
Authorised
- Dexamethasone sodium phosphate
Product identification
Medicine name:
DEXACORTYL
Active substance:
- Dexamethasone sodium phosphate
Target species:
-
Cattle
-
Pig
-
Equid
-
Goat
Route of administration:
-
Intramuscular use
-
Subcutaneous use
-
Periarticular use
-
Intravenous use
-
Intraarticular use
Product details
Active substance and strength:
-
Dexamethasone sodium phosphate2.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH02AB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Dopharma France S.A.S.
Marketing authorisation date:
Manufacturing sites for batch release:
- Dopharma France
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/9850725 4/1984
Date of authorisation status change:
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.
French (PDF)
Published on: 23/01/2023