BOVILIS IBR Marker
BOVILIS IBR Marker
Authorised
- Bovine herpesvirus 1, type 1, ge deleted, Inactivated
Product identification
Medicine name:
BOVILIS IBR Marker
Active substance:
- Bovine herpesvirus 1, type 1, ge deleted, Inactivated
Target species:
-
Cattle
Route of administration:
-
Nasal use
-
Intramuscular use
Product details
Active substance and strength:
-
Bovine herpesvirus 1, type 1, ge deleted, Inactivated5.70log10 tissue culture infective dose 501.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
-
Nasal use
- Cattle
-
Intramuscular use
- Cattle
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AD01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-2299
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.
Bulgarian (PDF)
Published on: 17/10/2023
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 17/10/2023
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