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Zydus Cadila receives final approval to launch two drugs in US market

Zydus Cadila said the drug will be produced at the group's formulations manufacturing facility at SEZ, Ahmedabad

Press Trust of India  |  New Delhi 

Zydus

has received final approval from the US health regulator to market Doxycycline Hyclate delayed-release tablets, used to treat bacterial infections.

has received the final approval from the (USFDA) to market the drug in the strengths of 75 mg, 100 mg and 150 mg, the company said in a BSE filing.

said the drug will be produced at the group's formulations manufacturing facility at SEZ, Ahmedabad.

The group has also received tentative approval for Febuxostat tablets in the strengths of 40 mg and 80 mg, used to treat hyperuricemia (constantly high levels of uric acid) in adults who have gout.

The group has more than 241 approvals, and so far filed over 340 abbreviated new drug applications (ANDAs) since it started filings in 2003-04.

Shares of Cadila Healthcare, the listed entity of the group, were trading 0.13 per cent lower at Rs 341.60 per scrip on BSE.

(Only the headline and picture of this report may have been reworked by the Business Standard staff; the rest of the content is auto-generated from a syndicated feed.)

First Published: Mon, December 24 2018. 11:45 IST
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