Skip to main content
Veterinary Medicines

CYPERMETHRIN FARMA

Authorised
  • Cypermethrin

Dettalji tal-prodott

Sustanza attiva / Qawwa:
  • Disponibbli biss fi English
    10.00
    gram(s)
    /
    100.00
    millilitre(s)
Forma farmaċewtika:
  • Soluzzjoni għall-ġilda
Withdrawal period by route of administration:
  • Cutaneous use
    • Cattle
      • Meat and offal
        28
        day
    • Sheep
      • Meat and offal
        28
        day
    • Dog
    • Cat
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
  • QP53AC08
Status tal-awtorizzazzjoni:
  • Valid
Authorised in:
  • Bulgaria
Deskrizzjoni tal-pakkett:

Tagħrif addizzjonali

Entitlement type:
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
  • Farma Vet OOD
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
  • Farmavet OOD
Awtorità responsabbli:
  • Bulgarian Agency For Food Safety
Numru tal-awtorizzazzjoni:
  • 0022-1921-07.01.2013
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.
Bulgarian (PDF)
Ippubblikat fuq: 24/01/2022
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."