Veterinary Medicines

Bactidiaryl Oral Powder

Authorised
  • Tetracycline hydrochloride
  • NEOMYCIN SULFATE
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Product identification

Medicine name:
Bactidiaryl Oral Powder
Active substance:
  • Tetracycline hydrochloride
  • NEOMYCIN SULFATE
Target species:
  • Cattle
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Tetracycline hydrochloride
    0.25
    gram(s)
    /
    100.00
    gram(s)
  • NEOMYCIN SULFATE
    500000.00
    international unit(s)
    /
    100.00
    gram(s)
Pharmaceutical form:
  • Oral powder
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        8
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01RA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • Aluminium foil pack containing 100g of an oral powder, 50 sachets per box.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Vetoquinol Ireland Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetoquinol Biowet Sp. z o.o.
  • Vetoquinol S.A.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10983/006/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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