NEMICINA 500.000 IU/g powder for use in drinking water/milk
NEMICINA 500.000 IU/g powder for use in drinking water/milk
Authorised
- NEOMYCIN SULFATE
Product identification
Medicine name:
NEMICINA 500.000 IU/g powder for use in drinking water/milk
NEMICINA 500.000 IU/g powder for use in drinking water/milk
Active substance:
- NEOMYCIN SULFATE
Target species:
-
Cattle (calf)
-
Pig
-
Chicken (broiler)
-
Turkey
-
Sheep (lamb)
-
Chicken (layer hen)
Route of administration:
-
In drinking water/milk use
-
In-feed use
Product details
Active substance and strength:
-
NEOMYCIN SULFATE500000.00/international unit(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Cattle (calf)
-
Meat and offal14day
-
-
Pig
-
Meat and offal14day
-
-
Chicken (broiler)
-
Meat and offal7day
-
-
Chicken (broiler)
-
Eggs0day
-
-
Turkey
-
Meat and offal7day
-
-
Turkey
-
Eggs0day
-
-
Sheep (lamb)
-
Meat and offal14day
-
-
Chicken (layer hen)
-
Meat and offal7day
-
-
Chicken (layer hen)
-
Eggs0day
-
-
-
In-feed use
-
Cattle (calf)
-
Meat and offal14day
-
-
Pig
-
Meat and offal14day
-
-
Chicken (broiler)
-
Meat and offal7day
-
-
Chicken (broiler)
-
Eggs0day
-
-
Turkey
-
Meat and offal7day
-
-
Turkey
-
Eggs0day
-
-
Sheep (lamb)
-
Meat and offal14day
-
-
Chicken (layer hen)
-
Meat and offal7day
-
-
Chicken (layer hen)
-
Eggs0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- 100 g bag
- 1 kg bag
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - known active substance (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- S P Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- S P Veterinaria S.A.
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-3317
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0436/001
Concerned member states:
-
Bulgaria
-
Cyprus
-
Hungary
-
Malta
-
Poland
-
Portugal
-
Romania
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: 24/07/2025
Bulgarian (PDF)
Published on: 21/07/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 21/07/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 21/07/2025
Combined File of all Documents
English (PDF)
Download Published on: 24/07/2025
eu-PUAR-esv0436001-dcp-nemicina-500.000-iu-g-powder-for-use-in-drinking-water-milk-en.pdf
English (PDF)
Download Published on: 29/09/2025