FATROXIMIN D.C. 100 mg/5 ml intramamálna masť
FATROXIMIN D.C. 100 mg/5 ml intramamálna masť
Awtorizzat
- Rifaximin
Informazzjoni dwar il-prodott
Isem tal-mediċina:
FATROXIMIN D.C. 100 mg/5 ml intramamálna masť
Sustanza attiva:
- Disponibbli biss fi Ingliż
Speċi li fuqhom ser jintuża l-prodott:
Metodu ta’ amministrazzjoni:
-
Użu intramammarju
Dettalji tal-prodott
Sustanza attiva / Qawwa:
-
Disponibbli biss fi Ingliż100.00/milligram(s)1.00Applicator
Forma farmaċewtika:
-
Ingwent intramammarju
Perjodu ta' rtirar skont ir-rotta tal-għoti:
-
Użu intramammarju
-
Cattle (dry cow)
-
Meat and offal0dayMeat and offal: without withdrawal period, The udder must be excluded from human consumption.
-
Milk0dayMilk: 0 days after calving if the length of dry standing is equal to or longer than 35 days. 35 days after administration if the duration of dry standing is less than 35 days.
-
-
Buffalo (female)
-
Meat and offal0dayMeat and offal: without withdrawal period, The udder must be excluded from human consumption.
-
Milk0dayMilk: 0 days after calving if the length of dry standing is equal to or longer than 35 days. 35 days after administration if the duration of dry standing is less than 35 days.
-
-
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QJ51XX01
Status tal-awtorizzazzjoni:
-
Valid
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- Fatro S.p.A.
Data tal-awtorizzazzjoni għall-kummerċjalizzazzjoni:
Siti ta’ manifattura b’rilaxx tal-lott:
- Fatro S.p.A.
Awtorità responsabbli:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Numru tal-awtorizzazzjoni:
- 96/0638/97-S
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 ’din il-lingwa (Malti). Tista’ ssibha b ’lingwa oħra hawn taħt.
Slovakk (PDF)
Ippubblikat fuq: 14/12/2021
