Veterinary Medicines

NEOSOL 500 000 IU/G POWDER FOR USE IN DRINKING WATER/MILK FOR CATTLE, CHICKENS, PIGS, DUCKS, TURKEYS, GEESE, QUAIL AND PARTRIDGES

Authorised
  • Neomycin
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Product identification

Medicine name:
NEOSOL 500 000 IU/G POWDER FOR USE IN DRINKING WATER/MILK FOR CATTLE, CHICKENS, PIGS, DUCKS, TURKEYS, GEESE, QUAIL AND PARTRIDGES
NeoSol 500.000 UI/g pulbere pentru administrare în apa de băut/lapte pentru bovine, găini, porci, rațe, curci, gâște, prepelițe și potârnichi
Active substance:
  • Neomycin
Target species:
  • Quail
  • Pig
  • Cattle (calf)
  • Partridge
  • Goose
  • Duck
  • Chicken
  • Turkey
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Neomycin
    500000.00
    international unit(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water/milk
Withdrawal period by route of administration:
  • Oral use
    • Quail
      • Meat and offal
        14
        day
      • Eggs
        0
        day
    • Pig
      • Meat and offal
        3
        day
    • Cattle (calf)
      • Meat and offal
        14
        day
    • Partridge
      • Meat and offal
        14
        day
      • Eggs
        0
        day
    • Goose
      • Meat and offal
        14
        day
      • Eggs
        0
        day
    • Duck
      • Meat and offal
        14
        day
      • Eggs
        0
        day
    • Chicken
      • Meat and offal
        14
        day
      • Eggs
        0
        day
    • Turkey
      • Meat and offal
        14
        day
      • Eggs
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Romania
Package description:
  • 100 g sachet
  • 1 kg bag

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
  • Huvepharma S.A.
Responsible authority:
  • Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
  • 250110
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0501/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)
Generic of:

Documents

Combined File of all Documents

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Romanian (PDF)
Published on: 25/07/2025
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15956 PuAR v3 final.pdf

English (PDF)
Published on: 18/08/2025
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