Veterinary Medicines

JODOFOAM Endofoam 200 mg/400 mg intrauterinná pena

Authorised
  • Iodine
  • Potassium iodide
Download as PDF

Identifikazzjoni tal-prodott

Isem tal-mediċina:
JODOFOAM Endofoam 200 mg/400 mg intrauterinná pena
Sustanza attiva:
Speċi li fuqhom ser jintuża l-prodott:
Metodu ta’ amministrazzjoni:
  • Użu għal ġo l-utru

Dettalji tal-prodott

Sustanza attiva / Qawwa:
  • Disponibbli biss fi English
    200.00
    milligram(s)
    /
    1.00
    Bottle
  • Disponibbli biss fi English
    400.00
    milligram(s)
    /
    1.00
    Bottle
Forma farmaċewtika:
Withdrawal period by route of administration:
  • Intrauterine use
    • Cattle (cow)
      • All relevant tissues
        0
        day
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
  • QG51AD30
Status legali tal-provvista:
Status tal-awtorizzazzjoni:
  • Valid
Authorised in:
  • Slovakia
Deskrizzjoni tal-pakkett:

Tagħrif addizzjonali

Entitlement type:
Bażi ġuridika tal-awtorizzazzjoni tal-prodott:
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
  • Tolnagro Kft.
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
  • Pernix Pharma Kft.
Awtorità responsabbli:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Numru tal-awtorizzazzjoni:
  • 96/0639/97-S
Data tal-bidla fl-istatus tal-awtorizzazzjoni:

Dokumenti

Combined File of all Documents

Dan id-dokument ma jeżistix f'dan il-lingwa (Malti). Tista 'ssibha f'lingwa oħra hawn taħt.
Slovak (PDF)
Ippubblikat fuq: 8/02/2024
Niżżel
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."