Nobivac RL suspensija injekcijām suņiem
Nobivac RL suspensija injekcijām suņiem
Authorised
- Rabies virus, strain Pasteur RIV, Inactivated
- Leptospira interrogans, serogroup Canicola, serovar Portland-vere, strain Ca-12-000, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Copenhageni, strain 820K, Inactivated
Product identification
Medicine name:
Nobivac RL suspensija injekcijām suņiem
Active substance:
- Rabies virus, strain Pasteur RIV, Inactivated
- Leptospira interrogans, serogroup Canicola, serovar Portland-vere, strain Ca-12-000, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Copenhageni, strain 820K, Inactivated
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Rabies virus, strain Pasteur RIV, Inactivated3.00international unit(s)1.00unit(s)
-
Leptospira interrogans, serogroup Canicola, serovar Portland-vere, strain Ca-12-000, Inactivated4.00Hamster protective Dose 80 % (Ph. Eur. Monograph)1.00unit(s)
-
Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Copenhageni, strain 820K, Inactivated4.00Hamster protective Dose 80 % (Ph. Eur. Monograph)1.00unit(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AL01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Package description:
- Available only in Latvian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- PVD
Authorisation number:
- V/NRP/96/0379
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.
Latvian (PDF)
Published on: 5/03/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 5/03/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 5/03/2024
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