Intraclox DC, intramaminė suspensija galvijams
Intraclox DC, intramaminė suspensija galvijams
Awtorizzat
- Cloxacillin
Identifikazzjoni tal-prodott
Isem tal-mediċina:
Intraclox DC, intramaminė suspensija galvijams
Sustanza attiva:
- Disponibbli biss fi English
Metodu ta’ amministrazzjoni:
-
Użu intramammarju
Dettalji tal-prodott
Sustanza attiva / Qawwa:
-
Disponibbli biss fi English500.00/milligram(s)1.00Syringe
Forma farmaċewtika:
-
Suspensjoni intramammarja
Withdrawal period by route of administration:
-
Użu intramammarju
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Cattle
-
Meat and offal28dayNot authorized for use in cattle, 35 days before calving.
-
Milk108hourFor human consumption, milk can be used only after 108 hours after calfing. If the cow calved 35 days before last treatment, their milk can be used for human consumption only after 35 days and 108 hours after last treatment. If the cow has hypocalcemia, the withdrawal period may be longer.
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-
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QJ51CF02
Status tal-awtorizzazzjoni:
-
Valid
Deskrizzjoni tal-pakkett:
- Disponibbli biss fi Lithuanian
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- Interchemie werken De Adelaar LT UAB
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
- Interchemie Werken De Adelaar Eesti AS
Awtorità responsabbli:
- State Food And Veterinary Service
Numru tal-awtorizzazzjoni:
- LT/2/20/2593/001
Data tal-bidla fl-istatus tal-awtorizzazzjoni:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Sommarju tal-karatteristiċi tal-prodott
Dan id-dokument ma jeżistix f'dan il-lingwa (Malti). Tista 'ssibha f'lingwa oħra hawn taħt.
Lithuanian (PDF)
Ippubblikat fuq: 21/03/2024
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