Sedivet 10 mg/ml solution injectable pour chevaux
Sedivet 10 mg/ml solution injectable pour chevaux
Authorised
- Romifidine hydrochloride
Product identification
Medicine name:
Sedivet 10 mg/ml solution injectable pour chevaux
Sedivet 10 mg/ml Injektionslösung
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 offal6day
-
Milkno withdrawal periodDo not use in animals producing milk for human consumption
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN05CM93
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Luxembourg
Available in:
-
Luxembourg
Package description:
- Sedivet 20 ml Vial Solution for injection
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 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:
- Ministere De La Sante Division De La Pharmacie Et Des Medicaments
Authorisation number:
- V 642/02/02/0728
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 23/03/2023
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 23/03/2023
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