This brand name is authorized in Austria, Estonia, Spain, Finland, France, Croatia, Ireland, Italy, Lithuania, Poland, United Kingdom
The drug QUOFENIX contains one active pharmaceutical ingredient (API):
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1
Delafloxacin
UNII N7V53U4U4T - DELAFLOXACIN MEGLUMINE
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Delafloxacin inhibits bacterial topoisomerase IV and DNA gyrase (topoisomerase II), enzymes required for bacterial DNA replication, transcription, repair, and recombination. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| QUOFENIX Tablet | European Medicines Agency (EU) | MPI, EU: SmPC | |
| QUOFENIX Powder for concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC code | Group title | Classification |
|---|---|---|
| J01MA23 | J Antiinfectives for systemic use → J01 Antibacterials for systemic use → J01M Quinolone antibacterials → J01MA Fluoroquinolones | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| Country: EE | Ravimiamet | Identifier(s): 1809109, 1809110, 1809121, 1809132, 1809143, 1809154, 1809165 |
| Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 1191393001, 1191393002 |
| Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 439060 |
| Country: FR | Base de données publique des médicaments | Identifier(s): 62560479, 69148567 |
| Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 387209, 387215 |
| Country: IE | Health Products Regulatory Authority | Identifier(s): 89106 |
| Country: IT | Agenzia del Farmaco | Identifier(s): 048404014, 048404026, 048404038, 048404040, 048404053, 048404065, 048404077 |
| Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1089137, 1089138, 1089139, 1089140, 1089141, 1089142, 1089143 |
| Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100429680, 100429705 |
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