Skip to main content
Veterinary Medicines

Bactidiaryl Oral Powder

Authorised
  • NEOMYCIN SULFATE
  • Tetracycline hydrochloride

Identifikazzjoni tal-prodott

Isem tal-mediċina:
Bactidiaryl Oral Powder
Sustanza attiva:
Metodu ta’ amministrazzjoni:
  • Użu orali

Dettalji tal-prodott

Sustanza attiva / Qawwa:
  • Disponibbli biss fi English
    500000.00
    international unit(s)
    /
    100.00
    gram(s)
  • Disponibbli biss fi English
    0.25
    gram(s)
    /
    100.00
    gram(s)
Forma farmaċewtika:
  • Trab orali
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        8
        day
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
  • QJ01RA90
Status tal-awtorizzazzjoni:
  • Valid
Authorised in:
Din l-informazzjoni mhijiex disponibbli għal dan il-prodott.
Deskrizzjoni tal-pakkett:

Tagħrif addizzjonali

Entitlement type:
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
  • Vetoquinol Ireland Limited
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
  • Vetoquinol Biowet Sp. z o.o.
  • VETOQUINOL SA
Awtorità responsabbli:
  • Health Products Regulatory Authority
Numru tal-awtorizzazzjoni:
  • VPA10983/006/001
Data tal-bidla fl-istatus tal-awtorizzazzjoni:

Dokumenti

Sommarju tal-karatteristiċi tal-prodott

Dan id-dokument ma jeżistix f'dan il-lingwa (Malti). Tista 'ssibha f'lingwa oħra hawn taħt.
English (PDF)
Ippubblikat fuq: 8/04/2022
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."