NUFLOR Swine 300 mg/ml Solution for injection
NUFLOR Swine 300 mg/ml Solution for injection
Authorised
- Florfenicol
Product identification
Medicine name:
NUFLOR Swine 300 mg/ml Solution for injection
Nuflor Swine 300 mg/ml Oplossing voor injectie
Nuflor Swine 300 mg/ml Solution injectable
Nuflor Swine 300 mg/ml Injektionslösung
Active substance:
- Florfenicol
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Florfenicol300.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal18day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01BA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Pack Size 20 ml colourless Type I glass vial closed with Grey bromobutyl rubber stopper with aluminium seal.
- Pack Size 50 ml colourless Type I glass vial closed with Grey bromobutyl rubber stopper with aluminium seal.
- Pack Size 100 ml colourless Type I glass vial closed with Grey bromobutyl rubber stopper with aluminium seal.
- Pack Size 250 ml colourless Type I glass vial closed with Grey bromobutyl rubber stopper with aluminium seal.
- Pack Size 500 ml colourless Type I glass vial closed with Grey bromobutyl rubber stopper with aluminium seal.
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:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Trirx Segre
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V220927
Date of authorisation status change:
Reference member state:
-
Italy
Procedure number:
- IT/V/0149/001
Concerned member states:
-
Austria
-
Belgium
-
Greece
-
Ireland
-
Luxembourg
-
Netherlands
-
Portugal
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Combined File of all Documents
English (PDF)
Download Published on: 22/12/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
