CIPROXIN

This brand name is authorized in Austria, Cyprus, Finland, Hong Kong, Ireland, Italy, Malta, Netherlands, New Zealand, United Kingdom

Active ingredients

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

1 Ciprofloxacin hydrochloride monohydrate
UNII 4BA73M5E37 - CIPROFLOXACIN HYDROCHLORIDE

Ciprofloxacin is a fluoroquinolone antibacterial agent. The bactericidal action of ciprofloxacin results from the inhibition of both type II topoisomerase (DNA-gyrase) and topoisomerase IV, required for bacterial DNA replication, transcription, repair and recombination.

Read about Ciprofloxacin

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
Ciproxin Tablets 250mg Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
J01MA02 Ciprofloxacin J Antiinfectives for systemic use → J01 Antibacterials for systemic use → J01M Quinolone antibacterials → J01MA Fluoroquinolones
Discover more medicines within J01MA02

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: FI Lรครคkealan turvallisuus- ja kehittรคmiskeskus Identifier(s): 195065
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 138499, 147117, 161495, 302678, 34926, 380958, 381253, 381394
Country: HK Department of Health Drug Office Identifier(s): 29934, 29936
Country: IE Health Products Regulatory Authority Identifier(s): 18341, 18953, 18961, 57738
Country: IT Agenzia del Farmaco Identifier(s): 026664019, 026664021, 026664096, 043270014, 044542013, 044941019, 045631013, 045858014
Country: MT Medicines Authority Identifier(s): MA639/01702, PI908/02903A
Country: NL Z-Index G-Standaard Identifier(s): 14177676, 14177684
Country: NL Z-Index G-Standaard, PRK Identifier(s): 50083, 50091
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 5027

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