Sun Pharma gets USFDA approval for CEQUA to treat dry eye

Published On 2018-08-17 07:29 GMT   |   Update On 2018-08-17 07:29 GMT

New Delhi: Sun Pharma has received approval from the US health regulator for CEQUA (cyclosporine ophthalmic solution), used to increase tear production in patients with keratoconjunctivitis sicca (dry eye).


Dry Eye Disease represents an area of high unmet medical need, with a significant number of patients who are currently untreated, Abhay Gandhi, CEO, North America, Sun Pharma.


"The the US Food and Drug Administration (USFDA) approval of CEQUA represents a long-awaited dry eye treatment option and is an important milestone in the development of Sun's Ophthalmics business," said he added.


"CEQUA (cyclosporine ophthalmic solution) 0.09 percent, for topical ophthalmic use will be commercialized in the US by Sun Ophthalmics, the branded ophthalmic division of Sun Pharma's wholly owned subsidiary," Sun Pharma said in a BSE filing.


CEQUA is dosed twice daily and will be available as a single-use vial.

Article Source : PTI

Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2020 Minerva Medical Treatment Pvt Ltd

Our comments section is governed by our Comments Policy . By posting comments at Medical Dialogues you automatically agree with our Comments Policy , Terms And Conditions and Privacy Policy .

Similar News