UK-based multinational pharmaceutical company Hikma Pharmaceuticals plc (LSE: HIK) (NASDAQ Dubai: HIK) (OTC: HKMPY) announced on Monday that it has introduced the first-of-its-kind, ready-to-use vancomycin premix with room-temperature stability under the brand name TYZAVAN (vancomycin injection, USP) in the United States.
TYZAVAN is offered in pre-filled ready-to-use bags designed to help hospitals, pharmacists, doctors, and nurses treat patients faster, more easily, and with reduced risk.
TYZAVAN, a glycopeptide antibacterial, is indicated for the treatment of infections such as septicaemia; infective endocarditis; skin and skin structure infections; bone infections; and lower respiratory tract infections.
According to Hikma, TYZAVAN is the only FDA-approved vancomycin injection available for adults and paediatric patients (aged one month and older) that can be stored at room temperature and used immediately, eliminating the need for compounding, thawing, assembly or activation to streamline preparation and accelerate treatment.
Roivant to announce Q3 2026 financial results
Avacta secures FDA clearance for second pre|CISION oncology programme
OncoHost receives BIG Innovation Award in Health category
Summit Therapeutics and GSK form collaboration to study ivonescimab combination therapy
Summit Therapeutics submits FDA application for ivonescimab in EGFR-mutated lung cancer
Antin to acquire clinical trial equipment provider Emsere
Merck completes acquisition of Cidara Therapeutics for USD9.2bn
Bambusa Therapeutics reports first patient dosed in proof-of-concept COPD trial
Kelun-Biotech lung cancer drug granted Breakthrough Therapy Designation in China
INOVIO's INO-3107 Biologics License Application accepted by US FDA
Sanofi and Regeneron's Dupixent gains Japan approval for paediatric asthma patients aged 6 to 11
Aqualung Therapeutics' Phase 2a lung fibrosis study approved by US FDA