POLIOVIN, suspension for injection for sheep, lambs, goats and kids
POLIOVIN, suspension for injection for sheep, lambs, goats and kids
Authorised
- Trueperella pyogenes, strain ATCC 9730, Inactivated
- STAPHYLOCOCCUS AUREUS
- Fusobacterium necrophorum, Inactivated
- Clostridium septicum, toxoid
- Clostridium novyi, type B, toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type C, beta toxoid
- Clostridium perfringens, type A, alpha toxoid
Product identification
Medicine name:
POLIOVIN, suspension for injection for sheep, lambs, goats and kids
Active substance:
- Trueperella pyogenes, strain ATCC 9730, Inactivated
- STAPHYLOCOCCUS AUREUS
- Fusobacterium necrophorum, Inactivated
- Clostridium septicum, toxoid
- Clostridium novyi, type B, toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type C, beta toxoid
- Clostridium perfringens, type A, alpha toxoid
Target species:
-
Sheep
-
Sheep (lamb)
-
Goat
-
Goat (dry adult)
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Trueperella pyogenes, strain ATCC 9730, Inactivated80.00/haemagglutinating units1.00Dose
-
STAPHYLOCOCCUS AUREUS0.50/haemagglutinating units1.00Dose
-
Fusobacterium necrophorum, Inactivated4.00/haemagglutinating units1.00Dose
-
Clostridium septicum, toxoid2.50/international unit(s)1.00Dose
-
Clostridium novyi, type B, toxoid3.50/international unit(s)1.00Dose
-
Clostridium perfringens, type D, epsilon toxoid5.00/international unit(s)1.00Dose
-
Clostridium perfringens, type C, beta toxoid10.00/international unit(s)1.00Dose
-
Clostridium perfringens, type A, alpha toxoid2.50/international unit(s)1.00Dose
Pharmaceutical form:
-
Suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI03AG
- QI04AG
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- Available only in Bulgarian
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:
- Bobal-Boyadjiev OOD
Marketing authorisation date:
Manufacturing sites for batch release:
- Bobal-Boyadjiev OOD
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-2758
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.
Bulgarian (PDF)
Published on: 15/05/2026
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 15/05/2026
Labelling
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 15/05/2026