Authorised

Product identification

Isem tal-mediċina:
Kaltetan forte, 458.4 mg/ml + 125 mg/ml + 20 mg/ml solution for infusion for horses, cattle and pigs
Kaltetan forte 458,4 mg/1 ml + 125 mg/1 ml + 20 mg/ml Roztwór do infuzji
Sustanza attiva:
Metodu ta’ amministrazzjoni:
  • Użu għal ġol-vini

Product details

Sustanza attiva / Qawwa:
  • Disponibbli biss fi English
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Disponibbli biss fi English
    125.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Disponibbli biss fi English
    458.40
    milligram(s)
    /
    1.00
    millilitre(s)
Forma farmaċewtika:
  • Soluzzjoni għall-infużjoni
Withdrawal period by route of administration:
  • Intravenous use
    • Horse
      • Milk
        5
        week
    • Cattle
      • Meat and offal
        5
        week
    • Pig
      • Meat and offal
        5
        week
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
  • QA12AX
Status tal-awtorizzazzjoni:
  • Valid
Authorised in:
  • Poland
Available in:
  • Poland
Deskrizzjoni tal-pakkett:

Additional information

Entitlement type:
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
  • Vet-Agro Multi-Trade Company Sp. z o.o.
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
  • Multi-Trade Company "Vet-Agro" Sp. z o.o.
Awtorità responsabbli:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Numru tal-awtorizzazzjoni:
  • 3172
Data tal-bidla fl-istatus tal-awtorizzazzjoni:
Numru tal-proċedura:
  • PL/V/0110/002

Source URL: https://medicines.health.europa.eu/veterinary/600000092622