FDA
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Why Late-Stage CNS, Oncology Assets Are Becoming the Hottest Targets in Biotech M&A
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Biogen Receives European Commission Approval for ZURZUVAEĀ® (zuranolone), the First and Only Treatment Approved for Women with Postpartum Depression in Europe
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Supernus Announces Paragraph IV ANDA Filings for QelbreeĀ®
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Supernus Pharma (SUPN) Announces Label Update for Qelbree
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Supernus Resubmits NDA for SPN-830 Apomorphine Infusion Device
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Stifel on Supernus Pharmaceuticals (SUPN): 'SPN-830 Approval Delayed Again, but Near-Term Impact Relatively Minor'
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Supernus Pharma (SUPN) Announces SPN-830 Apomorphine Infusion Device NDA Accepted for Review by FDA
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