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Medincell: U.S. Food and Drug Administration (FDA) Accepts Teva’s New Drug Application (NDA) for Olanzapine Extended-Release Injectable Suspension (TEV-'749) for the Once-Monthly Treatment of Schizophrenia in Adults

PARSIPPANY, N.J. & TEL AVIV, Israel & PARIS, February 20, 2026--Regulatory News: Teva Pharmaceuticals, a U.S. affiliate of Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA), and Medincell (Euronext: MEDCL), announced today that the U.S. Food and Drug Administration (FDA) has accepted its New Drug Application (NDA) for olanzapine extended-release injectable suspension (TEV-'749) for the treatment of schizophrenia in adults. TEV-'749 is designed to improve real-world treatment adherence an

articleMedincell SaFebruary 20, 20268/company/medincell-sa-1/news/medincell-us-food-and-drug-administration-fda-accepts-tevas-new-drug-application-nda-for-olanzapine-extended-release-injectable-suspension-tev-749-for-the-once-monthly-treatment-of-schizophrenia-in-adults-1
Medincell: U.S. Food and Drug Administration (FDA) Accepts Teva’s New Drug Application (NDA) for Olanzapine Extended-Release Injectable Suspension (TEV-'749) for the Once-Monthly Treatment of Schizophrenia in Adults

About this update from Medincell Sa

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Teva Pharmaceuticalssubcutaneous injectionMedincelltreatment adherenceadult patientsSOLARISschizophreniasafety profileLAIFood and Drug Administrationolanzapineefficacy