Indian pharma has little reason to fear Trump
US tariff threats on Indian generic drugs face significant obstacles. These duties could increase American healthcare costs and potentially cause shortages. Indian firms operate on low margins, making tariff absorption difficult. Recent US manu...
His pledge last month to apply a 100% levy on companies making off-patent medications by 2028 (rising to 200% a year later) unless they move production to the US faces formidable commercial and political obstacles. Instead of rushing to fire up new manufacturing facilities, the likes of Sun Pharmaceutical Industries Ltd. and Dr. Reddy's Laboratories Ltd. would be better off biding their time. The duties may never fully materialize.
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That’s because generic medicines play a crucial role in the healthcare system. Once patent protections on branded drugs expire, other manufacturers can produce equivalent versions, introducing competition that drives prices sharply lower. The difference can be enormous. According to one US Food & Drug Administration study, the price of an HIV medicine, Truvada, fell from about $50 to $3 a tablet shortly after generic versions became available.


And if the extra cost can’t be passed on to patients, some drugs could become unprofitable to produce, potentially leading to shortages — an even less acceptable trade-off than higher prices. A policy that would make the cheapest medicines much more expensive or unavailable would be politically unpalatable in 2028, a presidential election year.
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There’s another reason why Indian drugmakers should resist the pressure to set up manufacturing in the US. Recent history hardly makes a compelling case for investing there. Consider Dr. Reddy’s. In March last year, it shut a generic-drug factory in Shreveport, Louisiana, after years of losses. The plant, which had produced medicines including ibuprofen and aspirin, lacked a “clear path to profitability,” a spokesperson told a local newspaper.
For years, the generics trade had been moving out of the US. India's industry was born out of a 1970 decision to abolish pharmaceutical product patents, which encouraged domestic companies to master the art of reverse-engineering Western medicines. By the time India restored product patents in 2005, those companies had spent three decades building the expertise and scale that allowed them to pivot toward off-patent drugs for export. America's own embrace of generics came after a 1984 law opened the door for the FDA to approve the drugs on a shorter timeline, ultimately turning India into the pharmacy of the world.

Washington has legitimate reasons to worry about relying so heavily on overseas suppliers for essential drugs. But levies are an unusually blunt way of addressing that vulnerability. If the goal is greater resilience, then targeted incentives for strategically important medicines, diversified supply chains and guaranteed purchasing contracts would attack the problem more directly than taxing every imported generic.
The US spent four decades building a system that rewarded whoever could supply safe medicines most cheaply, and Asian companies became extraordinarily good at it. Until Washington proves it’s genuinely willing to undo all that, Indian drugmakers have little reason to panic.
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