NUFLOR Swine 300 mg/ml Solution for injection
NUFLOR Swine 300 mg/ml Solution for injection
Suspended
This information is not available for this product.
Product identification
Medicine name:
NUFLOR Swine 300 mg/ml Solution for injection
NUFLOR 300 mg/ml SOLUCION INYECTABLE PORCINO
Active substance:
This information is not available for this product.
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
This information is not available for this product.
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:
-
Suspended
Authorised in:
-
Spain
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:
- Merck Sharp & Dohme Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Trirx Segre
Responsible authority:
- Spanish Agency For Medicines And Health Products
Authorisation number:
- 1349 ESP
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0593/001
Concerned member states:
-
Austria
-
Belgium
-
Greece
-
Italy
-
Luxembourg
-
Netherlands
-
Portugal
-
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: 11/02/2022
Spanish (PDF)
Published on: 22/02/2023
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 22/02/2023
Labelling
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 22/02/2023
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