Dexrapid, 2mg/ml, Solution for injection
Dexrapid, 2mg/ml, Solution for injection
Authorised
- Dexamethasone
Product identification
Medicine name:
Dexrapid, 2mg/ml, Solution for injection
Active substance:
- Dexamethasone
Target species:
-
Horse
-
Pig
-
Cattle
-
Dog
-
Cat
Route of administration:
-
Intraarticular use
-
Intravenous use
-
Intramuscular use
Product details
Active substance and strength:
-
Dexamethasone2.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intraarticular use
-
Horse
-
Milkno withdrawal periodNot authorised for use in mares producing milk for human consumption.,
-
Meat and offal8day
-
-
-
Intravenous use
-
Horse
-
Milkno withdrawal periodNot authorised for use in mares producing milk for human consumption.,
-
Meat and offal8day
-
-
-
Intramuscular use
-
Horse
-
Milkno withdrawal periodNot authorised for use in mares producing milk for human consumption.,
-
Meat and offal8day
-
-
Pig
-
Meat and offal2day
-
-
Cattle
-
Milk72hour
-
Meat and offal8day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH02AB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
Available in:
-
Austria
Package description:
- Available only in German
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:
- Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetviva Richter GmbH
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 840391
Date of authorisation status change:
Reference member state:
-
Czechia
Procedure number:
- CZ/V/0167/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Denmark
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 26/08/2025
Updated on: 27/04/2026
Labelling
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 26/08/2025
Updated on: 27/04/2026
eu-puar-czv0167001-mr-dexrapid-en.pdf
English (PDF)
Download Published on: 14/03/2026