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Supernus Pharmaceuticals, Inc.

SUPN· NASDAQ
$41.92+0.19%
2026-10-30

Financials

Valuation Metrics

Supernus Pharmaceuticals, Inc.'s Market Cap is $2.43B. At end of 2025 it was $2.85B. Ranked #1841 of 3,118 in US market (top 59%), #670 of 1,474 on NASDAQ (top 45%), #114 of 265 in Pharmaceuticals, Biotechnology & Life Sciences (top 43%) by Market Cap.

Investment Metrics(as of 2026-10-30)

MetricValue
Size
Market Cap$2.43B
Revenue$865M
Net Income$-44M
Total Assets$1.40B
Net Assets$1.06B
Employees778
Value
P/B2.29x
P/S2.81x
EV/EBITDA35.65x
FCF Yield3.57%
Profitability
ROE-4.13%
ROA-3.14%
Op. Margin-3.51%
Revenue Growth26.93%
Financial Health
Debt Ratio31.55%
Total Debt$36M
FCF$87M
Cash$176M
Current Ratio2.49x
Net Debt/EBITDA-2.17x
Performance
1Y Return-25.81%
1M Return-2.60%
From 52W High-29.76%
1Y MDD-33.54%
Trading
Volume2,818,900 shares
Trading Value$118M
Per Share
EPS$-0.76
BPS$18.32

Company Info

CEO Mr. Jack A. Khattar M.B.A.
Employees 778
HQ Rockville, United States

Supernus Pharmaceuticals, Inc., a biopharmaceutical company, engages in the development and commercialization of products for the treatment of central nervous system (CNS) diseases in the United States. It offers Qelbree, a non-stimulant indicated for the treatment of attention-deficit hyperactivity disorder (ADHD); GOCOVRI for the treatment of dyskinesia and levodopa/carbidopa in patients with Parkinson's Disease (PD); Oxtellar XR, an extended-release oxcarbazepine product indicated for the monotherapy treatment of partial onset epilepsy seizures; and APOKYN for the acute and intermittent treatment of hypomobility or off episodes in patients with advanced PD. It also provides Trokendi XR, an extended release topiramate product indicated for the treatment of epilepsy, as well as for the prophylaxis of migraine headache; XADAGO for the treatment of levodopa/carbidopa in patients with PD experiencing off episodes; and MYOBLOC, a Type B toxin product indicated for the treatment of cervical dystonia and chronic sialorrhea. In addition, the company develops ONAPGO, which received FDA approval, for the treatment of motor fluctuations in adults with advanced PD; SPN-817, a first-in-class selective acetylcholinesterase inhibitor, which is in Phase 2 clinical trial, for the treatment of epilepsy, partial seizures, Dravet syndrome, and Lennox-Gaustaut syndrome; SPN-820, a small molecule in Phase 2 clinical trial for treating resistant depression; and SPN-443, a stimulant in Phase 1 trial for the treatment of ADHD/CNS. It markets and sells its products through pharmaceutical wholesalers, specialty pharmacies, and distributors. It has a development agreement with Navitor Inc. for the conduct of Phase 2 clinical program of SPN-820. Supernus Pharmaceuticals, Inc. was incorporated in 2005 and is based in Rockville, Maryland.