CYDECTIN TRICLAMOX 1 MG/ML + 50 MG/ML ORAL SOLUTION FOR SHEEP
CYDECTIN TRICLAMOX 1 MG/ML + 50 MG/ML ORAL SOLUTION FOR SHEEP
Awtorizzat
- Triclabendazole
- Moxidectin
Identifikazzjoni tal-prodott
Isem tal-mediċina:
CYDECTIN TRICLAMOX 1 MG/ML + 50 MG/ML ORAL SOLUTION FOR SHEEP
Cydectin Triclamox 1 mg/ml + 50 mg/ml orale oplossing voor schapen
Metodu ta’ amministrazzjoni:
-
Użu orali
Dettalji tal-prodott
Forma farmaċewtika:
-
Soluzzjoni orali
Withdrawal period by route of administration:
-
Użu orali
- Sheep
-
Meat and offal31day
-
Milkno withdrawal periodNot authorised for use in ewes producing milk intended for human consumption including during the dry period. Do not use within 1 year prior to the first lambing in ewes intended to produce milk for human consumption.
-
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QP54AB52
Status tal-awtorizzazzjoni:
-
Valid
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- Zoetis B.V.
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
- Zoetis Manufacturing & Research Spain S.L.
Awtorità responsabbli:
- Medicines Evaluation Board
Numru tal-awtorizzazzjoni:
- REG NL 102887
Data tal-bidla fl-istatus tal-awtorizzazzjoni:
Numru tal-proċedura:
- FR/V/0201/001
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.
Dutch (PDF)
Ippubblikat fuq: 28/03/2022
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