Fascionix 34% Inj.
Fascionix 34% Inj.
Authorised
- Nitroxinil
Product identification
Medicine name:
Fascionix 34% Inj.
Active substance:
- Nitroxinil
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Nitroxinil340.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal60daynot authorised for use in animals producing milk for human consumption including the dry period;not use during the last trimester of pregnancy in heifers which are intended to produce milk for human consumption
-
- Sheep
-
Meat and offal60daynot use within 1 year prior to the first lambing in ewes intended to produce milk for human consumption
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AG08
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Available in:
-
Bulgaria
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:
- Kepro B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Kepro B.V.
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-2157-16.01.2014
Date of authorisation status change:
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.
Bulgarian (PDF)
Published on: 1/09/2023
Updated on: 4/09/2023
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 1/09/2023
Updated on: 4/09/2023
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