USFDA gives tentative approval for Levomilnacipran extended-release capsules

The drug will be manufactured at the group’s formulation manufacturing facility at Moraiya, Ahmedabad, the statement said.

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USFDA Approval
USFDA Approval

Last Updated on October 15, 2024 by The Health Master

The United States Food and Drugs Administration (USFDA) has given tentative approval to Zydus Lifesciences to market Levomilnacipran extended-release capsules, 20 mg, 40 mg, 80 mg and 120 mg, according to a company statement.

Levomilnacipran is a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of major depressive disorder (MDD) in adults.

The drug will be manufactured at the group’s formulation manufacturing facility in Moraiya, Ahmedabad, the statement said.

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