OXYPHARM 110 mg/g prášok na perorálny roztok
OXYPHARM 110 mg/g prášok na perorálny roztok
Awtorizzat
- Oxytetracycline hydrochloride
Informazzjoni dwar il-prodott
Isem tal-mediċina:
OXYPHARM 110 mg/g prášok na perorálny roztok
Sustanza attiva:
- Disponibbli biss fi Ingliż
Speċi li fuqhom ser jintuża l-prodott:
Dettalji tal-prodott
Sustanza attiva / Qawwa:
-
Disponibbli biss fi Ingliż110.00/milligram(s)1.00gram(s)
Forma farmaċewtika:
-
Trab għal soluzzjoni orali
Perjodu ta' rtirar skont ir-rotta tal-għoti:
-
In drinking water use
-
Cattle (calf)
-
Meat and offal7day
-
-
Chicken
-
Meat and offal7dayDo not use in laying hens producing eggs for human consumption
-
-
Turkey
-
Meat and offal7dayDo not use in laying hens producing eggs for human consumption
-
-
Ornamental bird
-
Not applicable0dayNot applicable
-
-
Rabbit
-
Meat and offal7day
-
-
Dog
-
Not applicable0dayNot applicable
-
-
Cat
-
Not applicable0dayNot applicable
-
-
Fur animals
-
Not applicable0dayNot applicable
-
-
Pig
-
Meat and offal7day
-
-
Pigeon
-
Not applicable0dayDo not use in pigeons whose meat is intended for human consumption
-
-
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QJ01AA06
Status tal-awtorizzazzjoni:
-
Valid
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- Pharmagal spol. s r.o.
Data tal-awtorizzazzjoni għall-kummerċjalizzazzjoni:
Siti ta’ manifattura b’rilaxx tal-lott:
- Pharmagal spol. s r.o.
Awtorità responsabbli:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Numru tal-awtorizzazzjoni:
- 96/0593/96-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: 18/01/2022