RINI-SUIVAX T
RINI-SUIVAX T
Authorised
- Bordetella bronchiseptica, Inactivated
- Pasteurella multocida, Serotype D, Inactivated
- Pasteurella multocida, Serotype A, Inactivated
- Pasteurella multocida, toxoid
Product identification
Medicine name:
RINI-SUIVAX T
Active substance:
- Bordetella bronchiseptica, Inactivated
- Pasteurella multocida, Serotype D, Inactivated
- Pasteurella multocida, Serotype A, Inactivated
- Pasteurella multocida, toxoid
Target species:
-
Pig (female)
-
Pig (young female)
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Bordetella bronchiseptica, Inactivated32.00slow agglutination test unit(s)2.00millilitre(s)
-
Pasteurella multocida, Serotype D, Inactivated80.00percentage protection2.00millilitre(s)
-
Pasteurella multocida, Serotype A, Inactivated80.00percentage protection2.00millilitre(s)
-
Pasteurella multocida, toxoid2.00microgram(s)2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Pig (female)
-
Meat and offal0day
-
- Pig (young female)
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
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:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- MdS
Authorisation number:
This information is not available for this product.
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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Italian (PDF)
Published on: 19/09/2022
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