Zydus Cadila gets USFDA nod to market midodrine HCL tablets

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 received final approval from the USFDA to market Midodrine Hydrochloride Tablets (US RLD- ProAmatine Tablets) in the strengths of 2.5 mg, 5 mg, and 10 mg.

The drug is used for certain patients who have symptoms of low blood pressure when standing. This condition is also known as orthostatic hypotension.

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

The group now has 298 approvals and has so far filed over 390 ANDAs since the commencement of the filing process in FY 2003-04.

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