Nanotrim 464.2 mg/g + 100 mg/g powder for use in drinking water/milk for chickens, turkeys, pigs and cattle
Nanotrim 464.2 mg/g + 100 mg/g powder for use in drinking water/milk for chickens, turkeys, pigs and cattle
Authorised
- Sulfachlorpyridazine sodium
- Trimethoprim
Product identification
Medicine name:
Nanotrim 464.2 mg/g + 100 mg/g powder for use in drinking water/milk for chickens, turkeys, pigs and cattle
Nanotrim, 464,2 mg/g + 100 mg/g, milteliai, skirti naudoti su geriamuoju vandeniu ar pienu vištoms, kalakutams, kiaulėms ir galvijams
Active substance:
- Sulfachlorpyridazine sodium
- Trimethoprim
Target species:
-
Pig
-
Chicken
-
Turkey
-
Cattle (pre-ruminant)
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Sulfachlorpyridazine sodium500.00milligram(s)/gram1.00gram(s)
-
Trimethoprim100.00milligram(s)/gram1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Pig
-
Meat and offal7day
-
-
Chicken
-
Meat and offal3day
-
-
Turkey
-
Meat and offal9day
-
-
Cattle (pre-ruminant)
-
Meat and offal7day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EW12
Legal status of supply:
-
Medicinal product subject to medical prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Pillow sachet with 100 g made of polyethylene/aluminium/polyethylene terephthalate laminate
- 1k g resealable block-bottom zipped sachet made of polyethylene/aluminium/polyethylene terephthalate laminate
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 19(1) of Regulation (EU) 2019/6)
Marketing authorisation holder:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Biovet AD
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/25/2860/001-002
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0420/001
Concerned member states:
-
Austria
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
Lithuanian (PDF)
Published on: 9/05/2025
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