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Supernus Pharmaceuticals, Inc.

SUPN· NASDAQ
$44.38+1.84%
2026-06-18

Price Chart

Supernus Pharmaceuticals, Inc.+34.65%

Financials

※ FY = Fiscal Year

Investment Metrics(as of 2026-06-18)

MetricValue
Size
Market Cap$2.58B
Revenue$777M
Net Income$-29M
Total Assets$1.50B
Net Assets$1.08B
Employees778
Value
P/B2.39x
P/S3.32x
EV/EBITDA55.97x
FCF Yield3.19%
Profitability
ROE-2.69%
ROA-1.93%
Op. Margin-5.37%
Revenue Growth38.63%
Earnings Growth-152.19%
Financial Health
Debt Ratio39.37%
Total Debt$41M
FCF$82M
Cash$185M
Current Ratio1.96x
Net Debt/EBITDA-3.31x
Performance
1Y Return34.65%
1M Return-6.80%
From 52W High-25.64%
1Y MDD-23.54%
Trading
Volume902,835 shares
Trading Value$40M
Per Share
EPS$-0.67
BPS$18.51

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.