ALFADEXX 2 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, GOATS, PIGS, DOGS AND CATS
ALFADEXX 2 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, GOATS, PIGS, DOGS AND CATS
Authorised
- DEXAMETHASONE DISODIUM PHOSPHATE
Product identification
Medicine name:
ALFADEXX 2 MG/ML SOLUTION FOR INJECTION FOR HORSES, CATTLE, GOATS, PIGS, DOGS AND CATS
Alfadexx 2mg/ml Solution injectable
Alfadexx 2mg/ml Oplossing voor injectie
Alfadexx 2mg/ml Injektionslösung
Active substance:
- DEXAMETHASONE DISODIUM PHOSPHATE
Target species:
-
Cattle
-
Pig
-
Cat
-
Horse
-
Goat
-
Dog
Route of administration:
-
Intramuscular use
-
Subcutaneous use
-
Periarticular use
-
Intravenous use
-
Intraarticular use
Product details
Active substance and strength:
-
DEXAMETHASONE DISODIUM PHOSPHATE2.63milligram(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
-
-
Cat
-
Horse
-
Meat and offal8day
-
Milkno withdrawal periodNot authorized for use in horses producing milk for human consumption.
-
-
Goat
-
Meat and offal8day
-
Milk72hour
-
-
Dog
-
-
Subcutaneous use
-
Dog
-
Cat
-
-
Periarticular use
-
Horse
-
Meat and offal8day
-
Milkno withdrawal periodNot authorized for use in horses producing milk for human consumption.
-
-
-
Intravenous use
-
Cattle
-
Meat and offal8day
-
Milk72hour
-
-
Pig
-
Meat and offal6day
-
-
Cat
-
Horse
-
Meat and offal8day
-
Milkno withdrawal periodNot authorized for use in horses producing milk for human consumption.
-
-
Goat
-
Meat and offal8day
-
Milk72hour
-
-
Dog
-
-
Intraarticular use
-
Horse
-
Meat and offal8day
-
Milkno withdrawal periodNot authorized for use in horses producing milk 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:
-
Belgium
Available in:
-
Belgium
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:
- Alfasan Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Produlab Pharma B.V.
- Alfasan Nederland B.V.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V594373
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0430/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Summary of Product Characteristics
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Labelling
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