NOBIVAC RABIA
NOBIVAC RABIA
Authorised
- Rabies virus, strain Pasteur RIV, Inactivated
Product identification
Medicine name:
NOBIVAC RABIA
Active substance:
- Rabies virus, strain Pasteur RIV, Inactivated
Target species:
-
Cattle
-
Sheep
-
Horse
-
Dog
-
Cat
-
Ferret
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Rabies virus, strain Pasteur RIV, Inactivated2.00/international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal0day
-
- Sheep
-
Meat and offal0day
-
- Horse
-
Meat and offal0day
-
- Dog
- Cat
- Ferret
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
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:
- Merck Sharp & Dohme Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Spanish Agency For Medicines And Health Products
Authorisation number:
- 3229 ESP
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.
Spanish (PDF)
Published on: 24/04/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 24/04/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 24/04/2024
How useful was this page?:
