Sun Pharma arm recalls Bupropion hydrochloride ER tablets in US
The company is recalling 9,804 bottles of 150 mg strength and 744 bottles of 200 mg strength, the US health regulator stated.;
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New Delhi: Drug major Sun Pharma is recalling around 10,500 bottles of a generic drug meant for the treatment of major depressive disorders in the US market following a customer complaint.
According to the latest enforcement report of the US Food and Drug Administration (USFDA), the US arm of the domestic pharma major is recalling 10,548 bottles of bupropion hydrochloride extended-release tablets in the American market.
The drug is used to treat depression and prevent Seasonal Affective Disorder (SAD). It is also used to help people stop smoking.
As per the USFDA, the company is recalling the affected lot due to "presence of foreign substance: Customer complaint for the presence of dark, gritty substance found within the bottle, which was determined to be activated carbon from the desiccant canister inside the bottle".
Read also: Sun Pharma arm to unveil Bempedoic Acid under brand name Brillo in India
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