PropoFlo Plus, 10mg/ml, Emulsion for Injection
PropoFlo Plus, 10mg/ml, Emulsion for Injection
Authorised
- Propofol
Product identification
Medicine name:
PropoFlo Plus, 10mg/ml, Emulsion for Injection
PropoVet Multidose
Active substance:
- Propofol
Target species:
-
Dog
-
Cat
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
Propofol10.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN01AX10
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Package description:
- box containing 5 vials of 20 ml
- box containing 1 vial of 50 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Fresenius Kabi AB
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402063.00.00
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0324/001
Concerned member states:
-
Austria
-
Belgium
-
Denmark
-
Finland
-
France
-
Germany
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Norway
-
Portugal
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 3/12/2024
eu-PUAR-propoflo-plus--10mg-ml--emulsion-for-injection-en.pdf
English (PDF)
Download Published on: 6/04/2023
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