Rhemox 500 mg/g powder for use in drinking water for pigs, chicken broilers, duck broilers and turkeys for meat production
Rhemox 500 mg/g powder for use in drinking water for pigs, chicken broilers, duck broilers and turkeys for meat production
Awtorizzat
- Amoxicillin trihydrate
Informazzjoni dwar il-prodott
Isem tal-mediċina:
Rhemox 500 mg/g powder for use in drinking water for pigs, chicken broilers, duck broilers and turkeys for meat production
Rhemox 500 mg/g Poeder voor gebruik in drinkwater
Rhemox 500 mg/g Poudre pour administration dans l’eau de boisson
Rhemox 500 mg/g Pulver zum Eingeben über das Trinkwasser
Sustanza attiva:
- Disponibbli biss fi Ingliż
Speċi li fuqhom ser jintuża l-prodott:
Dettalji tal-prodott
Sustanza attiva / Qawwa:
-
Disponibbli biss fi Ingliż500.00/milligram(s)1.00gram(s)
Forma farmaċewtika:
-
Trab għal ma' l-ilma tax-xorb
Perjodu ta' rtirar skont ir-rotta tal-għoti:
-
In drinking water use
-
Pig
-
Meat and offal6day
-
-
Chicken (broiler)
-
Meat and offal1day
-
Eggsno withdrawal periodEggs: Not for use in birds producing or intended to produce eggs for human consumption. Do not use within 4 weeks of the start of the laying period.
-
-
Turkey (for meat production)
-
Meat and offal5day
-
Eggsno withdrawal periodEggs: Not for use in birds producing or intended to produce eggs for human consumption. Do not use within 4 weeks of the start of the laying period.
-
-
Duck (broiler)
-
Meat and offal9day
-
Eggsno withdrawal periodEggs: Not for use in birds producing or intended to produce eggs for human consumption. Do not use within 4 weeks of the start of the laying period.
-
-
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QJ01CA04
Status tal-awtorizzazzjoni:
-
Valid
Disponibbli fi:
-
Belgium
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- Industrial Veterinaria S.A.
Data tal-awtorizzazzjoni għall-kummerċjalizzazzjoni:
Siti ta’ manifattura b’rilaxx tal-lott:
- aniMedica Herstellungs GmbH
- Industria Italiana Integratori Trei S.p.A.
- Industrial Veterinaria S.A.
Awtorità responsabbli:
- Federal Agency For Medicines And Health Products
Numru tal-awtorizzazzjoni:
- BE-V493991
Data tal-bidla fl-istatus tal-awtorizzazzjoni:
Numru tal-proċedura:
- ES/V/0236/001
Stati Membri Kkonċernati:
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.
Fuljett ta’ tagħrif
Dan id-dokument ma jeżistix f'dan il-lingwa (Malti). Tista 'ssibha f'lingwa oħra hawn taħt.
Tikkettar
Dan id-dokument ma jeżistix f'dan il-lingwa (Malti). Tista 'ssibha f'lingwa oħra hawn taħt.
Combined File of all Documents
Dan id-dokument ma jeżistix f'dan il-lingwa (Malti). Tista 'ssibha f'lingwa oħra hawn taħt.
Ingliż (PDF)
Ippubblikat fuq: 24/07/2025
eu-PUAR-rhemox-500-mg-g-en.pdf
Ingliż (PDF)
Niżżel Ippubblikat fuq: 5/04/2023
