Veterinary Medicines

NEOXIVIT, pulbere orală

Authorised
  • NEOMYCIN SULFATE
  • Oxytetracycline hydrochloride
  • Thiamine
  • Riboflavin
  • Pyridoxine
  • Cyanocobalamin
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Product identification

Medicine name:
NEOXIVIT, pulbere orală
Active substance:
  • NEOMYCIN SULFATE
  • Oxytetracycline hydrochloride
  • Thiamine
  • Riboflavin
  • Pyridoxine
  • Cyanocobalamin
Target species:
  • Cattle (calf)
  • Sheep (lamb)
  • Pig (piglet)
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • NEOMYCIN SULFATE
    55.00
    milligram(s)
    /
    1.00
    gram(s)
  • Oxytetracycline hydrochloride
    55.00
    milligram(s)
    /
    1.00
    gram(s)
  • Thiamine
    6.00
    milligram(s)
    /
    1.00
    gram(s)
  • Riboflavin
    6.00
    milligram(s)
    /
    1.00
    gram(s)
  • Pyridoxine
    14.00
    milligram(s)
    /
    1.00
    gram(s)
  • Cyanocobalamin
    0.03
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Oral powder
Withdrawal period by route of administration:
  • In drinking water use
    • Cattle (calf)
      • Meat and offal
        7
        day
    • Sheep (lamb)
      • Meat and offal
        5
        day
    • Pig (piglet)
      • Meat and offal
        5
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11EA
  • QJ01AA06
  • QJ01GB05
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Romania
Available in:
  • Romania
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
  • Pasteur Filiala Filipesti S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Pasteur Filiala Filipesti S.A.
Responsible authority:
  • Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
  • 160249
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Romanian (PDF)
Published on: 19/07/2022
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