Excenel 50 mg/ml lyofilizát na prípravu injekčného roztoku
Excenel 50 mg/ml lyofilizát na prípravu injekčného roztoku
Authorised
- Ceftiofur sodium
Product identification
Medicine name:
Excenel 50 mg/ml lyofilizát na prípravu injekčného roztoku
Active substance:
- Ceftiofur sodium
Target species:
-
Cattle
-
Pig
-
Horse
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Ceftiofur sodium1060.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Lyophilisate for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal1dayMeat and offal 24 hours
-
Milk0daymilk zero days
-
-
Pig
-
Meat and offal2dayMeat and offal 48 hours
-
-
Horse
-
All relevant tissuesno withdrawal periodDo not use in horses whose meat is intended for human consumption
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01DD90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Available in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Ceska Republika s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Pfizer
- Pfizer Service Company
- Zoetis Belgium
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/013/05-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 31/10/2025