VETACORTYL
VETACORTYL
Authorised
- Prednisolone acetate
Product identification
Medicine name:
VETACORTYL
Active substance:
- Prednisolone acetate
Target species:
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Intrasynovial use
-
Subcutaneous use
-
Subconjunctival use
-
Intrathecal use
Product details
Active substance and strength:
-
Prednisolone acetate40.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Dog
-
Intrasynovial use
- Dog
-
Subcutaneous use
- Cat
-
Subconjunctival use
- Dog
-
Intrathecal use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH02AB04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- Available only in French
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetoquinol
Responsible authority:
- National Veterinary Medicines Agency
Authorisation number:
- FR/V/9097318 7/1983
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
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 4/04/2022
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