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Nobivac Respira Bb vet. suspension for injection in pre-filled syringe for dogs
  • Bordetella bronchiseptica, celms Bb7 92932, fimbrija
  • Valid
Authorised in these countries:
  • Latvia

Product identification

Medicine name:
Nobivac Respira Bb vet. suspension for injection in pre-filled syringe for dogs
Nobivac Respira Bb suspensija injekcijām pilnšļircē suņiem
Active substance and strength:
  • Bordetella bronchiseptica, celms Bb7 92932, fimbrija
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI06AE02
Authorisation number:
  • V/DCP/20/0055
Product identification number:
  • 59c83a28-af1d-409f-85c5-6faff45ee71b
Permanent identification number:
  • 600000060281

Product details

Pharmaceutical form:
  • Suspension for injection in pre-filled syringe
Withdrawal period by route of administration:
  • Subcutaneous use
    • Dog

Availability

Package description:
Manufacturing sites for batch release:
  • Intervet International B.V.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
  • DK/V/0123/001
Date of authorisation status change:
Authorisation country:
  • Latvia
Responsible authority:
  • PVD
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation issued:
Reference member state:
  • Denmark
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

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