Imrestor 5.5 mg/ml - Solution for injection in pre-filled syringe
Imrestor 5.5 mg/ml - Solution for injection in pre-filled syringe
Awtorizzat
- Pegbovigrastim
Identifikazzjoni tal-prodott
Isem tal-mediċina:
Imrestor 5.5 mg/ml - Solution for injection in pre-filled syringe
Sustanza attiva:
- Disponibbli biss fi English
Speċi li fuqhom ser jintuża l-prodott:
Metodu ta’ amministrazzjoni:
-
Użu għal taħt il-ġilda
Dettalji tal-prodott
Sustanza attiva / Qawwa:
-
Disponibbli biss fi English5.50milligram(s)1.00millilitre(s)
Forma farmaċewtika:
-
Soluzzjoni għall-injezzjoni
Withdrawal period by route of administration:
-
Użu għal taħt il-ġilda
- Cattle (heifer)
- Cattle (dairy cow)
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QL03AA90
Status tal-awtorizzazzjoni:
-
Valid
Authorised in:
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- Elanco GmbH
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
- Elanco France S.A.S
- Trirx Speke Limited
Awtorità responsabbli:
- European Commission
Numru tal-awtorizzazzjoni:
Din l-informazzjoni mhijiex disponibbli għal dan il-prodott.
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
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Niżżel Published on: 14/11/2022
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Slovenian (PDF)
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Spanish (PDF)
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Swedish (PDF)
Published on: 14/11/2022
ema-puar-imrestor-v-2763-par-en.pdf
English (PDF)
Niżżel Published on: 14/03/2023
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