VIGAMOX

This brand name is authorized in United States. It is also authorized in Brazil, Canada, Cyprus, Ecuador, Estonia, Finland, Hong Kong SAR China, Israel, Lithuania, Malta, Netherlands, Poland, Romania, Singapore, South Africa, Spain, Turkey.

Active ingredients

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

1
UNII C53598599T - MOXIFLOXACIN HYDROCHLORIDE
 

Moxifloxacin, a fourth-generation fluoroquinolone, has in vitro activity against a wide range of Gram-positive and Gram-negative pathogens. The bactericidal action of moxifloxacin results from the inhibition of both type II topoisomerases (DNA gyrase and topoisomerase IV) required for bacterial DNA replication, transcription and repair.

 
Read more about Moxifloxacin

Medicine classification

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

ATC Group Classification
S01AE07 S Sensory organs → S01 Ophthalmologicals → S01A Antiinfectives → S01AE Fluoroquinolones
Discover more medicines within S01AE07

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 500904201130317
CA Health Products and Food Branch 02252260
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 25.755-07-04
EE Ravimiamet 1338656
ES Centro de información online de medicamentos de la AEMPS 71576
FI Lääkealan turvallisuus- ja kehittämiskeskus 055164
HK Department of Health Drug Office 53158
IL מִשְׂרַד הַבְּרִיאוּת 4867
LT Valstybinė vaistų kontrolės tarnyba 1031060, 1092928
MT Medicines Authority MA1249/01901, PI908/15701A
NL Z-Index G-Standaard, PRK 90565
PL Rejestru Produktów Leczniczych 100217251, 100420986, 100433144, 100452342
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W63599001
SG Health Sciences Authority 12614P
TR İlaç ve Tıbbi Cihaz Kurumu 8699504612134
US FDA, National Drug Code 0065-4013, 50090-0859
ZA Health Products Regulatory Authority A40/15.1/0164

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