QUINSAIR

This brand name is authorized in Austria, Canada, Croatia, Estonia, Finland, Ireland, Italy, Lithuania, Netherlands, Poland, Spain, UK.

Active ingredients

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

1
UNII 6GNT3Y5LMF - LEVOFLOXACIN
 

Levofloxacin is a synthetic antibacterial agent of the fluoroquinolone class. As a fluoroquinolone antibacterial agent, levofloxacin acts on the DNA – DNA-gyrase complex and topoisomerase IV.

 
Read more about Levofloxacin

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 QUINSAIR Nebuliser solution 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
J01MA12 Levofloxacin J Antiinfectives for systemic use → J01 Antibacterials for systemic use → J01M Quinolone antibacterials → J01MA Fluoroquinolones
Discover more medicines within J01MA12

Authorization and marketing

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

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 02442302
EE Ravimiamet 1683121, 1849259
ES Centro de información online de medicamentos de la AEMPS 114973001
FI Lääkealan turvallisuus- ja kehittämiskeskus 427887
GB Medicines & Healthcare Products Regulatory Agency 325074
IE Health Products Regulatory Authority 88576
IT Agenzia del Farmaco 044034015, 044034027
LT Valstybinė vaistų kontrolės tarnyba 1076058, 1090526
NL Z-Index G-Standaard, PRK 132586
PL Rejestru Produktów Leczniczych 100342329

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