RABISIN suspenzija za injiciranje
RABISIN suspenzija za injiciranje
Authorised
- Rabies virus, strain G52, Inactivated
Product identification
Medicine name:
RABISIN suspenzija za injiciranje
Active substance:
- Rabies virus, strain G52, Inactivated
Target species:
-
Cattle
-
Sheep
-
Horse
-
Mink
-
Dog
-
Cat
Route of administration:
-
Subcutaneous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Rabies virus, strain G52, Inactivated1.00international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal, milk0dayMeso in organi živali namenjenih za prehrano ljudi: nič dni. Mleko živali, namenjeno za prehrano ljudi: nič dni.
-
- Sheep
-
Meat and offal, milk0dayMeso in organi živali namenjenih za prehrano ljudi: nič dni. Mleko živali, namenjeno za prehrano ljudi: nič dni.
-
- Horse
-
Meat and offal, milk0dayMeso in organi živali namenjenih za prehrano ljudi: nič dni. Mleko živali, namenjeno za prehrano ljudi: nič dni.
-
- Mink
- Dog
- Cat
-
Subcutaneous use
- Cattle
-
Meat and offal, milk0dayMeso in organi živali namenjenih za prehrano ljudi: nič dni. Mleko živali, namenjeno za prehrano ljudi: nič dni.
-
- Sheep
-
Meat and offal, milk0dayMeso in organi živali namenjenih za prehrano ljudi: nič dni. Mleko živali, namenjeno za prehrano ljudi: nič dni.
-
- Horse
-
Meat and offal, milk0dayMeso in organi živali namenjenih za prehrano ljudi: nič dni. Mleko živali, namenjeno za prehrano ljudi: nič dni.
-
- Mink
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Package description:
- Available only in slovenščina
- Available only in slovenščina
- Available only in slovenščina
- Available only in slovenščina
- Available only in slovenščina
- Available only in slovenščina
- Available only in slovenščina
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0290/001
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: 7/12/2021
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 7/12/2021
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