Orbenin extra dry cow 600 mg suspensie voor intramammair gebruik voor runderen
Orbenin extra dry cow 600 mg suspensie voor intramammair gebruik voor runderen
Awtorizzat
- Cloxacillin hemibenzathine
Identifikazzjoni tal-prodott
Isem tal-mediċina:
Orbenin extra dry cow 600 mg suspensie voor intramammair gebruik voor runderen
Sustanza attiva:
- Disponibbli biss fi English
Metodu ta’ amministrazzjoni:
-
Użu intramammarju
Dettalji tal-prodott
Sustanza attiva / Qawwa:
-
Disponibbli biss fi English600.00milligram(s)1.00Syringe
Forma farmaċewtika:
-
Suspensjoni intramammarja
Withdrawal period by route of administration:
-
Użu intramammarju
- Cattle
-
Milk44day44 days after last treatment, after calving within 42 days after treatment
-
Milk48hour48 hours after calving after more than 42 days after treatment
-
Meat and offalno withdrawal periodzero days
-
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QJ51CF02
Status tal-awtorizzazzjoni:
-
Valid
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- Zoetis B.V.
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
- Haupt Pharma Latina S.r.l.
Awtorità responsabbli:
- Medicines Evaluation Board
Numru tal-awtorizzazzjoni:
- REG NL 6901
Data tal-bidla fl-istatus tal-awtorizzazzjoni:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Combined File of all Documents
Dan id-dokument ma jeżistix f'dan il-lingwa (Malti). Tista 'ssibha f'lingwa oħra hawn taħt.
Dutch (PDF)
Ippubblikat fuq: 22/05/2024
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