प्राथमिक स्रोत रिकॉर्ड
Viatris ने FDA में अपने कम खुराक वाली एस्ट्रोजन साप्ताहिक पैच के लिए NDA देर से Q3 2025 में दाखिल किया। कंपनी को मध्य-2026 तक मंजूरी मिलने की उम्मीद है। यह संपत्ति को विकास से नियामक समीक्षा में आगे बढ़ाता है।
EX-99.1 2 exhibit991-3q25earningsrel.htm EX-99.1 Document Viatris Reports Third Quarter 2025 Results and Updates 2025 Financial Guidance • Delivers Total Revenues in Line With Expectations, Reflecting Strong Execution of its Global Business • Makes Late-Stage Pipeline Progress Including NDA Submission for Low-Dose Estrogen Weekly Patch • Acquires Aculys Pharma Including Rights to Pitolisant in Japan and Spydia® in Japan and Certain Other Markets in the Asia-Pacific Region • Returns More Than $920 Million of Capital to Shareholders Year-to-Date, Including $500 Million in Share Repurchases • Raises and Narrows 2025 Financial Guidance Ranges for Total Revenues, Adjusted EBITDA and Adjusted EPS [1] PITTSBURGH – November 6, 2025 – Viatris Inc. (Nasdaq: VTRS) today reported strong third