The company has received final approval from the United States Food and Drug Administration (USFDA) to market Cyproheptadine Hydrochloride tablets in the strength of 4 mg, Cadila Healthcare said in a BSE filing.
The drug will be produced at the group's formulation manufacturing facility at the pharma SEZ in Ahmedabad, it added.
The group now has around 115 approvals from USFDA and has so far filed 300 abbreviated new drug applications (ANDAs), Cadila Healthcare said.
Shares of Cadila Healthcare were trading 2.78 per cent down at Rs 445.10 on BSE.
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