CETRAXAL

This brand name is authorized in United States. It is also authorized in Ecuador, Finland, Israel, Poland, Singapore, Spain, UK.

Active ingredients

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

1
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 more about Ciprofloxacin

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 CETRAXAL Ear drops MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group Classification
S02AA15 Ciprofloxacin S Sensory organs → S02 Otologicals → S02A Antiinfectives → S02AA Antiinfectives
Discover more medicines within S02AA15

Authorization and marketing

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

Country Identification scheme Identifier(s)
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 984-MEE-0515
ES Centro de información online de medicamentos de la AEMPS 60883, 62602, 67925
FI Lääkealan turvallisuus- ja kehittämiskeskus 382449
GB Medicines & Healthcare Products Regulatory Agency 349407
IL מִשְׂרַד הַבְּרִיאוּת 8668
PL Rejestru Produktów Leczniczych 100279921
SG Health Sciences Authority 14596P, 14597P
US FDA, National Drug Code 66992-450

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