FLORFENICEN 300 mg/ml solution for injection for cattle, sheep and pig
FLORFENICEN 300 mg/ml solution for injection for cattle, sheep and pig
Authorised
- Florfenicol
- Florfenicol
Product identification
Medicine name:
FLORFENICEN 300 mg/ml solution for injection for cattle, sheep and pig
CENFLOR 300 mg/ml solução injetável para bovinos, ovinos e suínos
Active substance:
- Florfenicol
- Florfenicol
Target species:
-
Cattle
-
Sheep
-
Pig
-
Cattle
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Florfenicol300.00milligram(s)1.00millilitre(s)
-
Florfenicol300.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal30daypor via IM (a 20mg/kg de peso corporal, duas vezes)
-
Meat and offal44daypor via SC (a 40 mg/kg de peso corporal, uma vez)
-
-
Sheep
-
Meat and offal39dayNão administrar a fêmeas produtoras de leite destinado ao consumo humano, incluindo animais gestantes com intenção de produção de leite para consumo humano
-
-
Pig
-
Meat and offal18day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal44day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01BA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Package description:
- 250 ml polypropylene vials closed with a rubber-butyl septum and an aluminium capsule with blue Flip-Off sealing.
- 100 ml polypropylene vials closed with a rubber-butyl septum and an aluminium capsule with blue Flip-Off sealing.
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:
- Cenavisa S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Cenavisa S.L.
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 586/01/12DFVPT
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/0106/001
Concerned member states:
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 25/11/2021
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
Portuguese (PDF)
Published on: 14/10/2024
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