CANIGEN MHA2PLR
CANIGEN MHA2PLR
Suspended
- Canine distemper virus, strain Lederle VR128, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine parvovirus, strain Cornell 780916, Live
- Leptospira interrogans, serogroup Canicola, serovar Canicola, strain 601903, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain 601895, Inactivated
- Rabies virus, strain VP12, Inactivated
Product identification
Medicine name:
CANIGEN MHA2PLR
Active substance:
- Canine distemper virus, strain Lederle VR128, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine parvovirus, strain Cornell 780916, Live
- Leptospira interrogans, serogroup Canicola, serovar Canicola, strain 601903, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain 601895, Inactivated
- Rabies virus, strain VP12, Inactivated
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine distemper virus, strain Lederle VR128, Live5.00cell culture infective dose 501.00Dose
-
Canine adenovirus 2, strain Manhattan, Live6.00cell culture infective dose 501.00Dose
-
Canine parvovirus, strain Cornell 780916, Live7.00cell culture infective dose 501.00Dose
-
Leptospira interrogans, serogroup Canicola, serovar Canicola, strain 601903, Inactivated80.00percentage protection1.00Dose
-
Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain 601895, Inactivated80.00percentage protection1.00Dose
-
Rabies virus, strain VP12, Inactivated1.00international unit(s)1.00Dose
Pharmaceutical form:
-
Lyophilisate and suspension for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AJ05
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Suspended
Authorised 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:
- Virbac Espana S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
Responsible authority:
- The Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 3219 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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