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Veterinary Medicines

Acticarp 50 mg/ml, Solution for Injection

Authorised
  • Carprofen

Identifikazzjoni tal-prodott

Isem tal-mediċina:
Acticarp 50 mg/ml, Solution for Injection
Acticarp 50 mg/ml Roztwór do wstrzykiwań
Sustanza attiva:
Metodu ta’ amministrazzjoni:
  • Użu għal ġol-vini
  • Użu għal taħt il-ġilda

Dettalji tal-prodott

Sustanza attiva / Qawwa:
  • Disponibbli biss fi English
    50.00
    milligram(s)
    /
    1.00
    millilitre(s)
Forma farmaċewtika:
  • Soluzzjoni għall-injezzjoni
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Milk
        0
        hour
      • Meat and offal
        21
        day
  • Subcutaneous use
    • Cattle
      • Milk
        0
        hour
      • Meat and offal
        21
        day
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
  • QM01AE91
Status tal-awtorizzazzjoni:
  • Valid
Authorised in:
  • Poland
Deskrizzjoni tal-pakkett:

Tagħrif addizzjonali

Entitlement type:
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
  • Ecuphar
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
  • Laboratori Fundacio Dau
Awtorità responsabbli:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Numru tal-awtorizzazzjoni:
  • 2234
Numru tal-proċedura:
  • NL/V/0156/001
Stati Membri Kkonċernati:

Dokumenti

Sommarju tal-karatteristiċi tal-prodott

Dan id-dokument ma jeżistix f'dan il-lingwa (Malti). Tista 'ssibha f'lingwa oħra hawn taħt.
Polish (PDF)
Ippubblikat fuq: 4/02/2022

Fuljett ta’ tagħrif

Dan id-dokument ma jeżistix f'dan il-lingwa (Malti). Tista 'ssibha f'lingwa oħra hawn taħt.
Polish (PDF)
Ippubblikat fuq: 6/02/2023
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