ZYVOXID

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, France, Germany, Israel, Italy, Lithuania, Netherlands, Poland, Romania, South Africa, Spain, Tunisia, Turkey.

Active ingredients

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

1
UNII ISQ9I6J12J - LINEZOLID
 

Linezolid is a synthetic, antibacterial agent that belongs to a new class of antimicrobials, the oxazolidinones. It has in vitro activity against aerobic Gram-positive bacteria and anaerobic micro-organisms. Linezolid selectively inhibits bacterial protein synthesis via a unique mechanism of action.

 
Read more about Linezolid

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 ZYVOXID Tablet / Solution for Infusion / Granules for suspension MPI, Generic Health Products Regulatory Authority (ZA)

Medicine classification

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

ATC Group Classification
J01XX08 Linezolid J Antiinfectives for systemic use → J01 Antibacterials for systemic use → J01X Other antibacterials → J01XX Other antibacterials
Discover more medicines within J01XX08

Authorization and marketing

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

Country Identification scheme Identifier(s)
DE Bundesinstitut für Arzneimittel und Medizinprodukte 01640374, 01640405, 01640457, 10042347, 10042407
EE Ravimiamet 1013858, 1111330
ES Centro de información online de medicamentos de la AEMPS 64106, 64107, 64109
FR Base de données publique des médicaments 63095061, 63283095, 68311278
HR Agencija za lijekove i medicinske proizvode HR-H-202569569, HR-H-711194389
IL מִשְׂרַד הַבְּרִיאוּת 4399, 8621
IT Agenzia del Farmaco 035410226
LT Valstybinė vaistų kontrolės tarnyba 1015623, 1015625, 1015626
NL Z-Index G-Standaard 14681366
NL Z-Index G-Standaard, PRK 60151, 60186
PL Rejestru Produktów Leczniczych 100106340, 100106362
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W65053001, W65053002, W65054001, W65055001
TN Direction de la Pharmacie et du Médicament 10803052H, 10803053H
TR İlaç ve Tıbbi Cihaz Kurumu 8681308091031, 8699532098962
ZA Health Products Regulatory Authority 35/20.1.1/0310, 35/20.1.1/0311, 35/20.1.1/0312, 35/20.1.1/0313

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