NEOSKILAB Solution for injection
NEOSKILAB Solution for injection
Autoriseret
- NEOSTIGMINE METHYLSULFATE
Produktidentifikation
Lægemidlets navn:
NEOSKILAB 1.5 mg/ml solution for injection for cattle, sheep, goats and horses
NEOSKILAB Solution for injection
Aktiv substans:
- Kun tilgængelig på English
Dyrearter:
-
Kvæg
-
Får
-
Ged
-
Hest
Administrationsvej:
-
Intramuskulær anvendelse
-
Subkutan anvendelse
Produktoplysninger
Aktiv substans / Styrke:
-
Kun tilgængelig på English1.50milligram(s)1.00millilitre(s)
Lægemiddelform:
-
Injektionsvæske, opløsning
Withdrawal period by route of administration:
-
Intramuskulær anvendelse
- Kvæg
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Får
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Ged
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Hest
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
-
Subkutan anvendelse
- Kvæg
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Får
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Ged
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Hest
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
Anatomisk terapeutisk kemisk veterinær (ATCvet) kode:
- QN07AA01
Godkendelsesstatus:
-
Valid
Pakningsbeskrivelse:
- Kun tilgængelig på English
Yderligere oplysninger
Indehaver af markedsføringstilladelsen:
- Labiana Life Sciences S.A.
Marketing authorisation date:
Produktionssteder for batchfrigivelse:
- Labiana Life Sciences S.A.
Ansvarlig myndighed:
- Health Products Regulatory Authority
Markedsføringstilladelsesnummer:
- VPA10402/004/001
Dato for ændring af godkendelsesstatus:
Procedurenummer:
- ES/V/0389/001
Berørte medlemsstater:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenter
Produktresumé
Dette dokument findes ikke på dette sprog (dansk). Du kan finde det på et andet sprog nedenfor.
English (PDF)
Udgivet den: 12/04/2023
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