RHINANVAC CERDOS
RHINANVAC CERDOS
Authorised
- Bordetella bronchiseptica, strain S-4212, Inactivated
- Haemophilus parasuis, strain NCTC 4557, Inactivated
- Mycoplasma hyopneumoniae, strain VMRI-11, Inactivated
- Mannheimia haemolytica, serotype A2, strain NCTC 9380, Inactivated
- Pasteurella multocida, serotype D, strain P-934, Inactivated
- Pasteurella multocida, serotype D, dermonecrotic toxin, recombinant
Product identification
Medicine name:
RHINANVAC CERDOS
Active substance:
- Bordetella bronchiseptica, strain S-4212, Inactivated
- Haemophilus parasuis, strain NCTC 4557, Inactivated
- Mycoplasma hyopneumoniae, strain VMRI-11, Inactivated
- Mannheimia haemolytica, serotype A2, strain NCTC 9380, Inactivated
- Pasteurella multocida, serotype D, strain P-934, Inactivated
- Pasteurella multocida, serotype D, dermonecrotic toxin, recombinant
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Bordetella bronchiseptica, strain S-4212, Inactivated10.00antibody unit(s)1.00Dose
-
Haemophilus parasuis, strain NCTC 4557, Inactivated10.00enzyme-linked immunosorbent assay unit1.00Dose
-
Mycoplasma hyopneumoniae, strain VMRI-11, Inactivated10.00enzyme-linked immunosorbent assay unit1.00Dose
-
Mannheimia haemolytica, serotype A2, strain NCTC 9380, Inactivated10.00enzyme-linked immunosorbent assay unit1.00Dose
-
Pasteurella multocida, serotype D, strain P-934, Inactivated10.00enzyme-linked immunosorbent assay unit1.00Dose
-
Pasteurella multocida, serotype D, dermonecrotic toxin, recombinant10.00enzyme-linked immunosorbent assay unit1.00Dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Available in:
-
Spain
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:
- Laboratorios Syva S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Syva S.A.U.
Responsible authority:
- The Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 2879 ESP
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.
Spanish (PDF)
Published on: 9/11/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 9/11/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 9/11/2022
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