Zydus Cadila gets USFDA nod for drug to treat HIV infection

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

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USFDA Approval
USFDA Approval

Last Updated on October 17, 2024 by The Health Master

Zydus Cadila has received final approval from US Food and Drug Administration (USFDA) to market emtricitabine and tenofovir disoproxil fumarate tablets, 100 mg/150 mg, 133 mg/200 mg and 167 mg/250 mg.

The drug is used with other HIV medications to help control HIV infection. It helps to decrease the amount of HIV in one’s body so that the immune system can work better.

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

The group now has 319 approvals and has so far filed over 400 ANDAs since the commencement of the filing process in FY 2003-04.

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