Nobivac L+DHPPi lyofilisaat en suspensie voor suspensie voor injectie voor honden
Nobivac L+DHPPi lyofilisaat en suspensie voor suspensie voor injectie voor honden
Authorised
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Copenhageni, strain Ic-02-001, Inactivated
- Leptospira interrogans, serogroup Canicola, serovar Portland-vere, strain Ca-12-000, Inactivated
- Canine adenovirus 2, strain Manhattan LPV3, Live
- Canine parvovirus, strain 154, Live
- Canine parainfluenza virus, strain Cornell, Live
- Canine distemper virus, strain Onderstepoort, Live
Product identification
Medicine name:
Nobivac L+DHPPi lyofilisaat en suspensie voor suspensie voor injectie voor honden
Active substance:
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Copenhageni, strain Ic-02-001, Inactivated
- Leptospira interrogans, serogroup Canicola, serovar Portland-vere, strain Ca-12-000, Inactivated
- Canine adenovirus 2, strain Manhattan LPV3, Live
- Canine parvovirus, strain 154, Live
- Canine parainfluenza virus, strain Cornell, Live
- Canine distemper virus, strain Onderstepoort, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Copenhageni, strain Ic-02-001, Inactivated750.00unit(s)1.00Dose
-
Leptospira interrogans, serogroup Canicola, serovar Portland-vere, strain Ca-12-000, Inactivated1300.00unit(s)1.00Dose
-
Canine adenovirus 2, strain Manhattan LPV3, Live10000.00unit(s)1.00Dose
-
Canine parvovirus, strain 154, Live10000000.00unit(s)1.00Dose
-
Canine parainfluenza virus, strain Cornell, Live316228.00unit(s)1.00Dose
-
Canine distemper virus, strain Onderstepoort, Live10000.00unit(s)1.00Dose
Pharmaceutical form:
-
Lyophilisate for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AI02
Legal status of supply:
-
Medicinal product subject to medical 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:
- Intervet Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet Nederland B.V.
Responsible authority:
- MEB
Authorisation number:
- REG NL 9483
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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Dutch (PDF)
Published on: 27/07/2022
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