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Zydus receives US FDA marketing approval for cyproheptadine HCl tablets

Zydus Cadila, a Rs. 9,400 crore plus pharma giant from Ahmedabad, has received the final approval from the US Food and Drug Administration (FDA) to market cyproheptadine hydrochloride tablets USP, 4 mg.

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Description

 It is an antihistamine used to relieve allergy symptoms such as watery eyes, running nose, itching eyes or nose, sneezing, hives, and itching.

The drug will be produced at the group’s formulations manufacturing facility at the Pharma SEZ in Ahmedabad.

The group now has around 115 approvals and has so far filed over 300 ANDAs since the commencement of the filing process in FY 2003-04.

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Zydus receives us fda, cyproheptadine hcl tablets

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