WONDERCEF, 4200 mg/80 ml polvere e solvente per soluzione iniettabile per equidi non destinati alla produzione di alimenti per il consumo umano (NDPA)
WONDERCEF, 4200 mg/80 ml polvere e solvente per soluzione iniettabile per equidi non destinati alla produzione di alimenti per il consumo umano (NDPA)
Authorised
- Ceftiofur
Product identification
Medicine name:
WONDERCEF, 4200 mg/80 ml polvere e solvente per soluzione iniettabile per equidi non destinati alla produzione di alimenti per il consumo umano (NDPA)
Active substance:
- Ceftiofur
Target species:
-
Horse (non food-producing)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Ceftiofur4200.00/milligram(s)4.00gram(s)
Pharmaceutical form:
-
Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Horse (non food-producing)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01DD90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Package description:
- Available only in Italian
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:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- MdS
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Italian (PDF)
Published on: 16/11/2022
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