SONOVUE

This brand name is authorized in Austria, Brazil, Canada, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Italy, Lithuania, Poland, Romania, Singapore, Spain, UK.

Active ingredients

The drug SONOVUE contains one active pharmaceutical ingredient (API):

1
UNII WS7LR3I1D6 - SULFUR HEXAFLUORIDE
 

Sulphur hexafluoride is an inert, innocuous gas, poorly soluble in aqueous solutions. Sulphur hexafluoride is for use with ultrasound imaging to enhance the echogenicity of the blood, or of fluids in the urinary tract which results in an improved signal to noise ratio.

 
Read more about Sulfur hexafluoride

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 SONOVUE Powder and solvent for dispersion for injection MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
V08DA Ultrasound contrast media V Various → V08 Contrast media → V08D Ultrasound contrast media
Discover more medicines within V08DA
V08DA05 V Various → V08 Contrast media → V08D Ultrasound contrast media → V08DA Ultrasound contrast media
Discover more medicines within V08DA05

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 540714090002202
CA Health Products and Food Branch 02287684
EE Ravimiamet 1204771, 1880850
ES Centro de información online de medicamentos de la AEMPS 01177002
FI Lääkealan turvallisuus- ja kehittämiskeskus 005455
FR Base de données publique des médicaments 67884271
GB Medicines & Healthcare Products Regulatory Agency 81157
HK Department of Health Drug Office 51764
IL מִשְׂרַד הַבְּרִיאוּת 8188
IT Agenzia del Farmaco 035233016, 035233028
LT Valstybinė vaistų kontrolės tarnyba 1030827
PL Rejestru Produktów Leczniczych 100125632
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W51767001
SG Health Sciences Authority 12349P

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