PORCILIS PRRS LYOPHILISATE AND SOLVENT FOR SUSPENSION FOR INJECTION FOR PIGS
PORCILIS PRRS LYOPHILISATE AND SOLVENT FOR SUSPENSION FOR INJECTION FOR PIGS
Authorised
- Water for injection
- Porcine reproductive and respiratory syndrome virus, type 1, strain DV, Live
Product identification
Medicine name:
PORCILIS PRRS
PORCILIS PRRS LYOPHILISATE AND SOLVENT FOR SUSPENSION FOR INJECTION FOR PIGS
Active substance:
- Water for injection
- Porcine reproductive and respiratory syndrome virus, type 1, strain DV, Live
Target species:
-
Pig
Route of administration:
-
Intramuscular use
-
Intradermal use
Product details
Active substance and strength:
-
Water for injection1.00unit(s)1.00unit(s)
-
Porcine reproductive and respiratory syndrome virus, type 1, strain DV, Live10000.00tissue culture infective dose 501.00unit(s)
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
-
All relevant tissues0day
-
-
Intradermal use
- Pig
-
All relevant tissues0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AD03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription except for some pack sizes
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- National Veterinary Medicines Agency
Authorisation number:
- FR/V/5171050 7/2001
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0332/001
Concerned member states:
-
Austria
-
Belgium
-
Germany
-
Greece
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
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.
French (PDF)
Published on: 30/11/2023
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 27/02/2023
Combined File of all Documents
English (PDF)
Download Published on: 22/12/2023
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