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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.
Ingliż (PDF)
Ippubblikat fuq: 8/04/2022
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