Veterinary Medicines

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
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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 prašek za dajanje v vodo za pitje/mleko za piščance, purane, prašiče in govedo
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 sodium
    500.00
    milligram(s)/gram
    /
    1.00
    gram(s)
  • Trimethoprim
    100.00
    milligram(s)/gram
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water/milk
Withdrawal period by route of administration:
  • In drinking water/milk use
    • Pig
      • Meat and offal
        7
        day
    • Chicken
      • Meat and offal
        3
        day
    • Turkey
      • Meat and offal
        9
        day
    • Cattle (pre-ruminant)
      • Meat and offal
        7
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01EW12
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovenia
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:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • DC/V/0815/001
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

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 17/09/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 17/09/2025
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Labelling

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Slovenian (PDF)
Published on: 17/09/2025
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