Porcilis PRRS liofilizat in vehikel za raztopino za injiciranje za prašiče
Porcilis PRRS liofilizat in vehikel za raztopino za injiciranje za prašiče
Authorised
- Porcine reproductive and respiratory syndrome virus, type 1, strain DV, Live
Product identification
Medicine name:
Porcilis PRRS liofilizat in vehikel za raztopino za injiciranje za prašiče
Active substance:
- 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:
-
Porcine reproductive and respiratory syndrome virus, type 1, strain DV, Live10000.00tissue culture infective dose 501.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
-
Meat and offal0day
-
-
Intradermal use
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AD03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Package description:
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0269/001
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.
Slovenian (PDF)
Published on: 26/01/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 26/01/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 26/01/2024
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