Veterinary Medicines

Branzil Vet. premix 100 %

Authorised
  • Oxolinic acid
  • Oxolinic acid
  • Oxolinic acid
  • Oxolinic acid
  • Oxolinic acid
  • Oxolinic acid
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Product identification

Medicine name:
Branzil Vet. 100 % premix
Branzil Vet. premix 100 %
Active substance:
  • Oxolinic acid
  • Oxolinic acid
  • Oxolinic acid
  • Oxolinic acid
  • Oxolinic acid
  • Oxolinic acid
Target species:
  • Aquaculture animals
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Oxolinic acid
    1000.00
    milligram(s)
    /
    1000.00
    milligram(s)
  • Oxolinic acid
    1000.00
    milligram(s)
    /
    1000.00
    milligram(s)
  • Oxolinic acid
    1000.00
    milligram(s)
    /
    1000.00
    milligram(s)
  • Oxolinic acid
    1000.00
    milligram(s)
    /
    1000.00
    milligram(s)
  • Oxolinic acid
    1000.00
    milligram(s)
    /
    1000.00
    milligram(s)
  • Oxolinic acid
    1000.00
    milligram(s)
    /
    1000.00
    milligram(s)
Pharmaceutical form:
  • Premix for medicated feeding stuff
Withdrawal period by route of administration:
  • Oral use
    • Aquaculture animals
      • Meat and offal
        30
        day
      • Meat and offal
        30
        day
      • Meat and offal
        30
        day
      • Meat and offal
        30
        day
      • Meat and offal
        30
        day
      • Meat and offal
        30
        day
      • Meat and offal
        60
        day
      • Meat and offal
        60
        day
      • Meat and offal
        60
        day
      • Meat and offal
        60
        day
      • Meat and offal
        60
        day
      • Meat and offal
        60
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01MB05
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Denmark
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Aller Aqua A/S
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetrepharm ApS
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 14443
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Danish (, PREMIX)
Published on: 29/06/2023
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