FDA accepts Viatris sNDA for MR-141 presbyopia treatment review

Reuters02-25 19:59

FDA accepts Viatris sNDA for MR-141 presbyopia treatment review

The U.S. Food and Drug Administration has accepted Viatris Inc.’s supplemental New Drug Application for MR-141 (phentolamine ophthalmic solution 0.75%) for the treatment of presbyopia. The FDA set a PDUFA goal date of Oct. 17, 2026. The product is currently approved in the U.S. as Ryzumvi for reversal of pharmacologically induced mydriasis, and the filing seeks to expand its indication to presbyopia.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Viatris Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: 202602250659PR_NEWS_USPR_____NE94794) on February 25, 2026, and is solely responsible for the information contained therein.

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