Actavis gets FDA appro for 150mg bupropion

8 December 2008

Icelandic generics firm Actavis, which says it is not affected by its native country's economic crisis, has received US Food and Drug Administration approval to market a 150mg version of its bupropion HCl extended-release tablets, the equivalent of UK drug major GlaxoSmithKline's Wellbutrin.

Chief executive Doug Boothe said: "bupropion XL 150mg, together with 300mg, which was launched in August this year, offers significant value to our customers and patients."

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