USFDA gives approval for Lenalidomide capsules

Lenalidomide is used to treat various types of cancers by slowing or stopping the growth of cancer cells.

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USFDA Approval
USFDA Approval

Last Updated on October 9, 2024 by The Health Master

Ahmedabad: Zydus Lifesciences has received approval from the United States Food and Drug Administration (USFDA) to market Lenalidomide Capsules, USP 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg, and 25 mg.

The company has received final approvals for 5 mg, 10 mg, 15 mg, and 25 mg strengths and tentative approvals for 2.5 mg and 20 mg strengths.

Lenalidomide is used to treat various types of cancers by slowing or stopping the growth of cancer cells.

It is also used to treat anemia in patients with certain blood and bone marrow disorders.

The drug will be manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ, India.

According to IQVIA MAT July 2022, Lenalidomide had annual sales of USD 2.86 bn in the United States.

The product will soon be launched in the US market.

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