Prednisolone 2.5 % Oplossing voor injectie
Prednisolone 2.5 % Oplossing voor injectie
Authorised
- Prednisolone
Product identification
Medicine name:
Prednisolone 2.5 % Oplossing voor injectie
Prednisolone 2.5 % Solution injectable
Prednisolone 2.5 % Injektionslösung
Active substance:
- Prednisolone
Target species:
-
Dog
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Prednisolone25.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH02AB04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Prednisolone 50 ml Vial Solution for injection
- Prednisolone 25 ml Vial Solution for injection
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
- VMD N.V.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V104167
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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Package Leaflet
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Labelling
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