Danilon equidos 1.5 g Granules for horses and ponies
Danilon equidos 1.5 g Granules for horses and ponies
Mhux awtorizzat
- Suxibuzone
Identifikazzjoni tal-prodott
Isem tal-mediċina:
Danilon equidos 1.5 g Granules for horses and ponies
Danilon equidos 1,5 g kyrni fyrir hesta og smáhesta (pony).
Sustanza attiva:
- Disponibbli biss fi English
Speċi li fuqhom ser jintuża l-prodott:
Metodu ta’ amministrazzjoni:
-
Użu ta’ mediċina mħallta ma’ l-ikel
Dettalji tal-prodott
Sustanza attiva / Qawwa:
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Disponibbli biss fi English1.50gram(s)10.00gram(s)
Forma farmaċewtika:
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Granijiet
Withdrawal period by route of administration:
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Użu ta’ mediċina mħallta ma’ l-ikel
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Horse
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Meat and offalno withdrawal periodNot to be used in animals intended for human consumption. Treated horses may never be slaughtered for human consumption. The horse must have been declared as not intended for human consumption under national horse passport legislation.
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Milkno withdrawal periodNot to be used in animals intended for human consumption. Treated horses may never be slaughtered for human consumption. The horse must have been declared as not intended for human consumption under national horse passport legislation.
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Horse (pony)
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Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QM01AA90
Status tal-awtorizzazzjoni:
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Surrendered
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- Ecuphar Veterinaria S.L.U.
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
- Esteve Pharmaceuticals S.A.
Awtorità responsabbli:
- Icelandic Medicines Agency
Numru tal-awtorizzazzjoni:
- IS/2/11/016/01
Data tal-bidla fl-istatus tal-awtorizzazzjoni:
Numru tal-proċedura:
- DE/V/0192/001
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.
English (PDF)
Ippubblikat fuq: 10/08/2022
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