Aurobindo receives tentative FDA OK for abacavir sulfate/lamivudine
This article was originally published in Scrip
Executive Summary
Aurobindo Pharmahas received tentative approval from the US FDAto manufacture and market abacavir sulfate/lamivudine tablets 600mg/300mg, a generic version of GlaxoSmithKline's Epzicom tablets. The product was reviewed under the President's emergency plan for AIDS relief (PEPFAR), Aurobindo informed the Bombay Stock Exchange. The product represents Aurobindo's 76th ANDA approval by the FDA.
You may also be interested in...
IGI Bets On Trispecific Antibody To Make Inroads Into Big Pharma Myeloma Turf
Ichnos Glenmark Innovation’s president and CEO talks to Scrip about the promising activity profile of the alliance’s early stage trispecific antibody versus Janssen’s teclistamab and also maintains that the setback for Gilead’s magrolimab hasn’t eclipsed prospects for its bispecific antibody.
How Sanofi Is ‘Playing To Win’ In India, Watch Diabetes Space
Sanofi India managing director Rodolfo Hrosz talks to Scrip about the company’s refreshed India strategy including in the competitive diabetes segment, which is expected to see a flurry of new product activity. While Soliqua has hit the market, all eyes are also on Novo Nordisk’s Awiqli and Cipla’s partnered inhaled insulin in the wings.
Asia Deal Watch: Nippon Shinyaku Takes On Intractable Rare Disease With MiNA
Plus deals involving Incyte/CMS, Biocytogen/ABL, Bharat/Biofabri/Bilthoven, Dr. Reddy’s/Pharmazz, Veeda/Heads, Sosei Heptares/GSK, BioGeometry/Sanyou, Ono/Sibylla and Teijin/BioProjet