DEXAVEX 2 mg/ml solution for injection
DEXAVEX 2 mg/ml solution for injection
Authorised
- Dexamethasone sodium phosphate
Product identification
Medicine name:
DEXAVEX 2 mg/ml solution for injection
Active substance:
- Dexamethasone sodium phosphate
Target species:
-
Cattle
-
Horse
-
Pig
-
Dog
-
Goat
-
Cat
Route of administration:
-
Intramuscular use
-
Intraarticular use
-
Intravenous 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
-
-
Horse
-
Meat and offal8day
-
Milkno withdrawal periodNot authorised for use in horses producing milk for human consumption
-
-
Pig
-
Meat and offal2day
-
-
Goat
-
Meat and offal8day
-
Milk72hour
-
-
Cattle
-
Meat and offal8day
-
Milk72hour
-
-
Horse
-
Meat and offal8day
-
Milkno withdrawal periodNot authorised for use in horses producing milk for human consumption
-
-
Goat
-
Meat and offal8day
-
Milk72hour
-
-
-
Intraarticular use
-
Horse
-
Meat and offal8day
-
Milkno withdrawal periodNot authorised for use in horses producing milk for human consumption
-
-
Horse
-
Meat and offal8day
-
Milkno withdrawal periodNot authorised for use in horses producing milk for human consumption
-
-
-
Intravenous use
-
Horse
-
Meat and offal8day
-
Milkno withdrawal periodNot authorised for use in horses producing milk for human consumption
-
-
Goat
-
Meat and offal8day
-
Milk72hour
-
-
Horse
-
Meat and offal8day
-
Milkno withdrawal periodNot authorised for use in horses producing milk for human consumption
-
-
Goat
-
Meat and offal8day
-
Milk72hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH02AB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Package description:
- box containing 10 vials of 50 ml
- box containing 1 vial of 50 ml
- Box containing 1 vial of 100 ml
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:
- S P Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- S P Veterinaria S.A.
Responsible authority:
- Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 2693 ESP
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0271/001
Concerned member states:
-
Portugal
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 24/07/2025
Summary of Product Characteristics
English (PDF)
Download Published on: 27/06/2024
Spanish (PDF)
Published on: 15/04/2025