10 Aug 2026
Lupin received US FDA approval for Sodium Zirconium Cyclosilicate for Oral Suspension in 5 gram and 10 gram packets, bioequivalent to AstraZeneca's Lokelma.
The reference brand did 568 million dollars of US sales in the twelve months to June 2026, and this is Lupin's second US approval inside a fortnight after Sugammadex on 31 July.
31 Jul 2026
Lupin received full US FDA approval for Sugammadex Injection and launched it in the United States the same day, against Merck's Bridion.
Lupin held only a tentative approval on the molecule as recently as 31 March 2026, so it converted to approval and launch inside four months on a large branded anaesthesia market.
21 Jul 2026
Lupin licensed two oncology programs, LNP7457 and LNP8701, to the newly formed Kaveri Therapeutics for 1.6 million dollars, taking an 82.2 percent equity stake in exchange.
Both candidates posted positive data at ASCO in 2025 and 2026. The spin-out moves expensive late-stage trials off the parent balance sheet while Lupin keeps most of the upside.
17 Jun 2026
Lupin launched Azilsartan Medoxomil tablets in the United States.
The cardiovascular generic extends Lupin's US portfolio in a therapy area with steady prescription demand, supporting the franchise that drives its US revenue.
25 May 2026
Lupin received Chinese regulatory approval for Oseltamivir Phosphate Oral Suspension, an antiviral for influenza treatment.
China is a high-volume antiviral market. This adds a new geographic revenue stream to Lupin's branded generic portfolio.
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