Sedivet vet. 10 mg/ml Injektionsvätska, lösning
Sedivet vet. 10 mg/ml Injektionsvätska, lösning
Authorised
- Romifidine hydrochloride
Product identification
Medicine name:
Sedivet vet. 10 mg/ml Injektionsvätska, lösning
Active substance:
- Romifidine hydrochloride
Target species:
-
Horse
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
Romifidine hydrochloride10.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
- Horse
-
Meat and offal10dayEj tillåtet för användning till lakterande djur som producerar mjölk för human konsumtion.
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN05CM93
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Sweden
Package description:
- Available only in Swedish
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Labiana Life Sciences S.A.
Responsible authority:
- Swedish Medical Products Agency
Authorisation number:
- 11753
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 28/06/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 20/04/2023
How useful was this page?:
