FIXR PRRS inac
FIXR PRRS inac
Authorised
- Porcine reproductive and respiratory syndrome virus, type 2, strain Bio-61, Inactivated
- Porcine reproductive and respiratory syndrome virus, type 1, strain Bio-60, Inactivated
Product identification
Medicine name:
FIXR PRRS inac
FIXR PRRS Inac Emulsie voor injectie
FIXR PRRS Inac Emulsion injectable
FIXR PRRS Inac Emulsion zur Injektion
Active substance:
- Porcine reproductive and respiratory syndrome virus, type 2, strain Bio-61, Inactivated
- Porcine reproductive and respiratory syndrome virus, type 1, strain Bio-60, Inactivated
Target species:
-
Pig (sow)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Porcine reproductive and respiratory syndrome virus, type 2, strain Bio-61, Inactivated1.00unit(s)1.00Dose
-
Porcine reproductive and respiratory syndrome virus, type 1, strain Bio-60, Inactivated1.00unit(s)1.00Dose
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig (sow)
-
All relevant tissues0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AA05
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- 1 × 10 ml (1 x 5 doses ) - glass vials hydrolytic class I or plastic HDPE vials closed with chlorobutyl rubber stoppers, sealed with aluminum caps in a cardboard box.
- 10 x 10 ml (10 x 5 doses) - glass vials hydrolytic class I or plastic HDPE vials closed with chlorobutyl rubber stoppers, sealed with aluminum caps in a cardboard box with a grid or PVC box.
- 1 × 50 ml (1 x 25 doses) - glass vials hydrolytic class II or plastic HDPE vials closed with chlorobutyl rubber stoppers, sealed with aluminum caps in a cardboard box.
- 1 × 100 ml (1 x 50 doses) - glass vials hydrolytic class II or plastic HDPE vials closed with chlorobutyl rubber stoppers, sealed with aluminum caps in a cardboard box.
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:
- Kernfarm B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- FAMHP
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0342/001
Concerned member states:
-
Belgium
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.
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
How useful was this page?: