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Zydus Cadila receives final approval for Cyproheptadine Hydrochloride tablets USP

Zydus Cadila has received the final approval from the USFDA to market Cyproheptadine Hydrochloride Tablets USP, 4 mg. 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.

Zydus Cadila is an innovative, global pharmaceutical company that discovers, develops, manufactures and markets a broad range of healthcare therapies.

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