Salicifarm 1000 mg/g powder for use in drinking water/milk for cattle and pigs
Salicifarm 1000 mg/g powder for use in drinking water/milk for cattle and pigs
Authorised
- Sodium salicylate
Product identification
Medicine name:
Salicifarm 1000 mg/g powder for use in drinking water/milk for cattle and pigs
Nobilis MS Live Żywy, atenuowany szczep MS1. M. synoviae: ≥10^6,5 i ≤ 10^8,0 CFU 11 - Colony Forming Units - jednostki tworzące kolonie Liofilizat i rozpuszczalnik do sporządzania zawiesiny na oczy i nozdrza
Active substance:
- Sodium salicylate
Target species:
-
Cattle (calf)
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Sodium salicylate1000.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
Oral use
-
Cattle (calf)
-
Meat and offalno withdrawal periodZero days
-
-
Pig
-
Meat and offalno withdrawal periodZero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN02BA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Package description:
- 500 g container of high density polyethylene
- 1 kg container of high density polyethylene
- 1 kg multilayer bag (PET-aluminium-Polythene)
- 5 kg multilayer bag (PET-aluminium-Polythene)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Chemifarma S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Chemifarma S.p.A.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 3455
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0432/001
Concerned member states:
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
France
-
Greece
-
Hungary
-
Italy
-
Lithuania
-
Poland
-
Portugal
-
Romania
Generic of:
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.
Polish (PDF)
Published on: 1/12/2025
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 1/12/2025