First generic versions of Strattera approved in the USA

31 May 2017
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Several drugmakers have simultaneously received US Food and Drug Administration approval for copycat versions of Strattera (atomoxetine), a treatment for attention-deficit/hyperactivity disorder in pediatric and adult patients.

The drug has consistently brought in over half a billion dollars in revenue for American pharma major Eli Lilly (NYSE: LLY).

The newly approved challengers are Canada’s Apotex, Israel’s Teva Pharmaceuticals (NYSE: TEVA) and Indian drugmakers Aurobindo Pharma (BSE: 524804) and Glenmark Pharmaceuticals (BSE: 532296).

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