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Why India’s first US FDA-approved antibiotic can change the fight against superbugs

Dr Habil F. Khorakiwala on Wockhardt’s homegrown antibiotic, ZAYNICH, on the significance of the approval and how the drug could change treatment options for antimicrobial resistance

Dr Habil F. KhorakiwalaDr Habil F. Khorakiwala. (Source: Express Photo)
Written by: Purnima Sah
7 min readJun 24, 2026 11:17 AM IST First published on: Jun 24, 2026 at 10:00 AM IST

For decades, India has been known as the world’s pharmacy, building a formidable global presence in generic medicines and vaccines. Much of that success stems from the country’s 1970 patent regime, which enabled Indian companies to manufacture medicines discovered elsewhere through alternative production processes. The model transformed access to affordable medicines, nurtured domestic drugmakers and helped India emerge as the world’s largest supplier of generic drugs. But it also meant that few companies ventured into the far riskier business of discovering new medicines — a process that can take more than a decade, cost billions of dollars and still end in failure.

That is what makes Wockhardt’s latest achievement noteworthy. On May 30, 2026, the US Food and Drug Administration (FDA) approved ZAYNICH™ (cefepime and zidebactam), a novel intravenous antibiotic for treating adults with complicated urinary tract infections caused by susceptible Gram-negative bacteria. This is a group of bacteria that have a distinctive outer cell wall, which makes them harder to kill with antibiotics.

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