IBR marker żywy Liofilizat i rozpuszczalnik do sporządzania zawiesiny do wstrzykiwań
IBR marker żywy Liofilizat i rozpuszczalnik do sporządzania zawiesiny do wstrzykiwań
Authorised
- Infectious Bovine rhinotracheitis virus, strain GK/D gE gene-deleted, Inactivated
Product identification
Medicine name:
IBR marker żywy Liofilizat i rozpuszczalnik do sporządzania zawiesiny do wstrzykiwań
Active substance:
- Infectious Bovine rhinotracheitis virus, strain GK/D gE gene-deleted, Inactivated
Target species:
-
Cattle
Route of administration:
-
Nasal use
-
Intramuscular use
Product details
Active substance and strength:
-
Infectious Bovine rhinotracheitis virus, strain GK/D gE gene-deleted, Inactivated19952600.00tissue culture infective dose 502.00millilitre(s)
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Nasal use
- Cattle
-
Meat and offal5week
-
-
Intramuscular use
- Cattle
-
Meat and offal5week
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AD02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Package description:
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2211
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.
Polish (PDF)
Published on: 4/02/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 4/02/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 26/04/2022
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