Porcilis M Hyo ID ONCE emulsion for injection for pigs
Porcilis M Hyo ID ONCE emulsion for injection for pigs
Authorised
- Mycoplasma hyopneumoniae, strain 11, Inactivated
Product identification
Medicine name:
Porcilis M Hyo ID ONCE emulsion for injection for pigs
Porcilis M Hyo ID ONCE injektionsvæske, emulsion
Active substance:
- Mycoplasma hyopneumoniae, strain 11, Inactivated
Target species:
-
Pig
Route of administration:
-
Intradermal use
Product details
Active substance and strength:
-
Mycoplasma hyopneumoniae, strain 11, Inactivated
Pharmaceutical form:
-
Emulsion for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB13
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Package description:
- Cardboard box with 10 PET vials of 20 ml (100 doses)
- Cardboard box with 5 PET vials of 20 ml (100 doses)
- Cardboard box with 1 PET vial of 20 ml (100 doses)
- Cardboard box with 10 glass vials of 20 ml (100 doses)
- Cardboard box with 10 glass vials of 10 ml (50 doses)
- Cardboard box with 5 glass vials of 20 ml (100 doses)
- Cardboard box with 5 glass vials of 10 ml (50 doses)
- Cardboard box with 1 glass vial of 20 ml (100 doses)
- Cardboard box with 1 glass vial of 10 ml (50 doses)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 47083
Date of authorisation status change:
Reference member state:
-
Hungary
Procedure number:
- HU/V/0109/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
France
-
Germany
-
Greece
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
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.
Danish (PDF)
Published on: 29/06/2023
Combined File of all Documents
English (PDF)
Download Published on: 27/08/2025