Parvoruvax
Parvoruvax
Authorised
- Porcine parvovirus, strain K22, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, Inactivated
Product identification
Medicine name:
Parvoruvax
Active substance:
- Porcine parvovirus, strain K22, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Porcine parvovirus, strain K22, Inactivated1.00/unit(s)1.00Dose
-
Erysipelothrix rhusiopathiae, serotype 2, Inactivated1.00/unit(s)1.00Dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offalno withdrawal periodWithdrawal period = zero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AL01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- CEVA Sante Animale B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva-Phylaxia Zrt.
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 4217
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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Published on: 9/12/2024