DOXIPULVIS 500 MG/G POWDER FOR USE IN DRINKING WATER / MILK
DOXIPULVIS 500 MG/G POWDER FOR USE IN DRINKING WATER / MILK
Awtorizzat
- Doxycycline hyclate
Informazzjoni dwar il-prodott
Isem tal-mediċina:
DOXIPULVIS 500 MG/G POWDER FOR USE IN DRINKING WATER / MILK
DOXIPULVIS 500 mg/g pulbere pentru utilizare în apa de băut/lapte
Sustanza attiva:
- Disponibbli biss fi Ingliż
Speċi li fuqhom ser jintuża l-prodott:
Metodu ta’ amministrazzjoni:
-
Użu orali
Dettalji tal-prodott
Sustanza attiva / Qawwa:
-
Disponibbli biss fi Ingliż577.10/milligram(s)1.00gram(s)
Perjodu ta' rtirar skont ir-rotta tal-għoti:
-
Użu orali
-
Turkey
-
Meat and offal12day
-
Eggsno withdrawal periodNot for use in birds producing eggs for human consumption.
Do not use within 4 weeks before the start of the laying period.
-
-
Pig
-
Meat and offal6day
-
-
Cattle (calf)
-
Meat and offal14day
-
-
Chicken
-
Meat and offal7day
-
Eggsno withdrawal periodNot for use in birds producing eggs for human consumption.
Do not use within 4 weeks before the start of the laying period.
-
-
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QJ01AA02
Status tal-awtorizzazzjoni:
-
Valid
Disponibbli fi:
-
Romania
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- S P Veterinaria S.A.
Data tal-awtorizzazzjoni għall-kummerċjalizzazzjoni:
Siti ta’ manifattura b’rilaxx tal-lott:
- S P Veterinaria S.A.
Awtorità responsabbli:
- Institute For Control Of Biological Products And Veterinary Medicines
Numru tal-awtorizzazzjoni:
- 220018
Data tal-bidla fl-istatus tal-awtorizzazzjoni:
Numru tal-proċedura:
- FR/V/0298/001
Stati Membri Kkonċernati:
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.
Rumen (PDF)
Ippubblikat fuq: 11/02/2026