CEVAXEL 50 MG/ML POWDER AND SOLVENT FOR SOLUTION FOR INJECTION FOR CATTLE AND PIGS
CEVAXEL 50 MG/ML POWDER AND SOLVENT FOR SOLUTION FOR INJECTION FOR CATTLE AND PIGS
Not authorised
- Ceftiofur hydrochloride
- Water for injection
Product identification
Medicine name:
CEVAXEL 50 MG/ML POWDER AND SOLVENT FOR SOLUTION FOR INJECTION FOR CATTLE AND PIGS
Active substance:
- Ceftiofur hydrochloride
- Water for injection
Target species:
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Ceftiofur hydrochloride53.50/milligram(s)1.00millilitre(s)
-
Water for injection1.00/millilitre(s)1.00millilitre(s)
Pharmaceutical form:
-
Powder and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal2day
-
Milk0day
-
-
Pig
-
Meat and offal2day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01DD90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Estonia
Package description:
- Box containing 1 vial of Cevaxel 50 mg/ml 1 g and box containing a vial of 20 ml solvent
- Box containing 1 vial of Cevaxel 50 mg/ml, 4 g and box containing a vial of 80 ml solvent
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:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
Responsible authority:
- State Agency Of Medicines
Authorisation number:
- 1522
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0177/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Estonian (PDF)
Published on: 9/05/2022