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Zydus Cadila gets tentative USFDA approval to market arthritis drug

The tablets will be manufactured at the group's manufacturing facility at SEZ, Ahmedabad, Zydus Cadila said.

Press Trust of India  |  New Delhi 

Cadila Healthcare
Cadila Healthcare

Drug firm on Saturday said it has received a tentative approval from the US health regulator to market generic Apremilast tablets.

The company has received the tentative approval from the United States Food and Drug Administration (USFDA) to market the tablets in the strengths of 10 mg, 20 mg, and 30 mg, said in a filing to BSE.

This medication is used to treat psoriatic and moderate to severe plaque psoriasis. It is also used to treat mouth sores in people who have Behcet's disease, it added.

The tablets will be manufactured at the group's manufacturing facility at SEZ, Ahmedabad, said.

The group now has 276 approvals and has so far filed over 360 ANDAs since the commencement of its filing process, it added.

First Published: Sat, November 16 2019. 19:20 IST
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