Nuflor Minidose 450 mg/ml solution for injection for cattle
Nuflor Minidose 450 mg/ml solution for injection for cattle
Not authorised
- Florfenicol
Product identification
Medicine name:
Nuflor Minidose 450 mg/ml solution for injection for cattle
NUFLOR MINIDOSE 450 mg/ml, raztopina za injiciranje za govedo
Active substance:
- Florfenicol
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Florfenicol450.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal64day
-
Milkno withdrawal periodNot permitted for use in lactating animals producing milk for human consumption.
-
-
Intramuscular use
- Cattle
-
Meat and offal37day
-
Milkno withdrawal periodNot permitted for use in lactating animals producing milk for human consumption.
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01BA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Slovenia
Package description:
- (ID3): 1 unspecified outer container with 1 Vial (Glass) with 250 millilitre(s) (250 millilitre(s))
- (ID2): 1 unspecified outer container with 1 Vial (Glass) with 100 millilitre(s) (100 millilitre(s))
- (ID1): 1 unspecified outer container with 1 Vial (Glass) with 50 millilitre(s) (50 millilitre(s))
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:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International GmbH
- Trirx Segre
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- DC/V/0241/004
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0122/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 4/05/2023
Labelling
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 4/05/2023
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 4/05/2023
Combined File of all Documents
English (PDF)
Download Published on: 11/01/2023
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