HIPRADOG SEVEN lyophilizate for suspension for injection with solvent for dogs
HIPRADOG SEVEN lyophilizate for suspension for injection with solvent for dogs
Authorised
- Leptospira interrogans, serovar Canicola, Inactivated
- Leptospira interrogans, serovar Icterohaemorrhagiae, Inactivated
- Canine parainfluenza virus, strain Penn 103/70, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine distemper virus, strain Lederle, Live
- Canine parvovirus, strain Cornell 780916, Live
Product identification
Medicine name:
HIPRADOG SEVEN lyophilizate for suspension for injection with solvent for dogs
Active substance:
- Leptospira interrogans, serovar Canicola, Inactivated
- Leptospira interrogans, serovar Icterohaemorrhagiae, Inactivated
- Canine parainfluenza virus, strain Penn 103/70, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine distemper virus, strain Lederle, Live
- Canine parvovirus, strain Cornell 780916, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Leptospira interrogans, serovar Canicola, Inactivated10.00/billion organisms1.00Dose
-
Leptospira interrogans, serovar Icterohaemorrhagiae, Inactivated10.00/billion organisms1.00Dose
-
Canine parainfluenza virus, strain Penn 103/70, Live5.00/log10 50% tissue culture infectious dose1.00Dose
-
Canine adenovirus 2, strain Manhattan, Live4.00/log10 50% tissue culture infectious dose1.00Dose
-
Canine distemper virus, strain Lederle, Live4.00/log10 50% tissue culture infectious dose1.00Dose
-
Canine parvovirus, strain Cornell 780916, Live6.00/log10 50% tissue culture infectious dose1.00Dose
Pharmaceutical form:
-
Suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AI02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- Available only in Bulgarian
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 Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Hipra S.A.
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-2756
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.
Bulgarian (PDF)
Published on: 15/05/2026
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 15/05/2026
Labelling
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 15/05/2026