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3 Generic Drug Stocks to Watch Amid Trade War Jitters & Inflation Woes

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While 2025 began on a positive note for the pharmaceutical industry, things have taken a sharp turn amid escalating fears of a global trade war. While Trump had initially exempted pharmaceuticals from proposed tariffs, he recently mentioned at an event that he will soon announce a ‘major’ tariff on pharmaceutical imports, adding uncertainty to the sector.

Trump’s push to bring drug manufacturing back to the United States has sparked concerns across the industry, particularly for generic drugmakers already operating under tight margins. If implemented, these tariffs could further squeeze profitability as these companies rely heavily on overseas production.

In response, generic drugmakers like Dr. Reddy’s Laboratories RDY, Sandoz SDZNY and Teva Pharmaceuticals TEVA are likely to focus on grasping the opportunity to be the ‘first to market’ their generic drugs. This allows them to enjoy market exclusivity for a limited period and generate profits. These firms are also undertaking cost optimization policies to improve margins and increase the efficiency of available resources.

Industry Description

The Medical - Generic Drugs industry comprises companies that develop and market chemically/biologically identical versions of a brand-name drug once patents expire, providing exclusivity to branded drugs. These drugs can be divided into generic and biosimilar categories based on their composition. The generic segment is controlled by a few large drugmakers and generic units of large pharma companies. Several smaller companies also develop generic versions of branded drugs, significantly cheaper than original drugs. Competition in this segment is stiff, resulting in thin margins for manufacturing companies. A few companies in this industry have some branded drugs in their portfolio, helping them tap a higher-margin market.

3 Trends Shaping the Future of the Generic Drugs Industry

Loss of Patent Exclusivity of Branded Drugs: Generic drugmakers mainly rely on the loss of patent exclusivity of branded drugs. They apply to the FDA for the approval of their generic or biosimilar version of branded drugs, which have lost patent protection. A company may launch an authorized generic version of a branded product, gaining exclusivity over other generic versions of the same drug for several months. This is advantageous to generic players, especially in the case of complex generics, which require significant R&D investments and expertise compared with traditional generics. These generic drugmakers even face litigations to market the generic version of the branded drugs.