Biocan R suspensija injekcijām
Biocan R suspensija injekcijām
Authorised
- Rabies virus, strain SAD Vnukovo-32, Inactivated
Product identification
Medicine name:
Biocan R suspensija injekcijām
Active substance:
- Rabies virus, strain SAD Vnukovo-32, Inactivated
Target species:
-
Ferret
-
Cat
-
Dog
-
Horse
-
Sheep
-
Goat
-
Cattle
-
Pig
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Rabies virus, strain SAD Vnukovo-32, Inactivated2.00/international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Horse
-
All relevant tissues0day
-
-
Sheep
-
All relevant tissues0day
-
-
Goat
-
All relevant tissues0day
-
-
Cattle
-
All relevant tissues0day
-
-
Pig
-
All relevant tissues0day
-
-
-
Intramuscular use
-
Cattle
-
All relevant tissues0day
-
-
Horse
-
All relevant tissues0day
-
-
Goat
-
All relevant tissues0day
-
-
Pig
-
All relevant tissues0day
-
-
Sheep
-
All relevant tissues0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Package description:
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- Available only in Latvian
- 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:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/03/1552
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Latvian (PDF)
Published on: 23/04/2026