Biofel PCHR, Emulsion for injection
Biofel PCHR, Emulsion for injection
Authorised
- Feline calicivirus, strain FCV F9 Bio-8, Inactivated
- Feline panleucopenia virus, strain FPV Bio 7, Inactivated
- Felid herpesvirus 1, strain FHV-1 Bio-9, Inactivated
- Rabies virus, strain SAD Vnukovo-32, Inactivated
Product identification
Medicine name:
Biofel PCHR, Emulsion for injection
Biofel PCHR injekčná emulzia pre mačky
Active substance:
- Feline calicivirus, strain FCV F9 Bio-8, Inactivated
- Feline panleucopenia virus, strain FPV Bio 7, Inactivated
- Felid herpesvirus 1, strain FHV-1 Bio-9, Inactivated
- Rabies virus, strain SAD Vnukovo-32, Inactivated
Target species:
-
Cat
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Feline calicivirus, strain FCV F9 Bio-8, Inactivated1.00/percent1.00Dose
-
Feline panleucopenia virus, strain FPV Bio 7, Inactivated1.00/relative potency1.00Dose
-
Felid herpesvirus 1, strain FHV-1 Bio-9, Inactivated1.00/relative potency1.00Dose
-
Rabies virus, strain SAD Vnukovo-32, Inactivated1.00/international unit(s)1.00Dose
Pharmaceutical form:
-
Emulsion for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI06AA09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Package description:
- Glass Vial 1 x 2.0 Dose
- Glass Vial 1 x 10.0 Dose
- Glass Vial 1 x 20.0 Dose
- Glass Vial 1 x 100.0 Dose
- Glass Vial 1 x 5.0 Dose
- Glass Vial 5 x 5.0 Dose
- Glass Vial 10 x 5.0 Dose
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/015/MR/19-S
Date of authorisation status change:
Reference member state:
-
Czechia
Procedure number:
- CZ/V/0157/001
Concerned member states:
-
Slovakia
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 3/03/2022