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Key facts: FDA Accepts Viatris' MR-141 Application; Q4 Results Due Soon
The FDA has accepted Viatris, Inc.'s application for MR-141 (Phentolamine Ophthalmic Solution 0.75%) to treat presbyopia, with a decision expected by October 17, 2026. Viatris is also preparing to report its fourth-quarter results soon, which will include updates on its 2026 forecast and the performance of its generic drugs business.