Supernus Pharmaceuticals, Inc.

NasdaqGM SUPN

Supernus Pharmaceuticals, Inc. EBIT Margin for the Trailing 12 Months (TTM) ending September 30, 2024: 11.95%

Supernus Pharmaceuticals, Inc. EBIT Margin is 11.95% for the Trailing 12 Months (TTM) ending September 30, 2024, a 129.87% change year over year. EBIT ratio is the ratio of EBIT to revenue, measuring a company's operating profitability without considering non-operating income or expenses.
  • Supernus Pharmaceuticals, Inc. EBIT Margin for the Trailing 12 Months (TTM) ending September 30, 2023 was 5.20%, a 42.77% change year over year.
  • Supernus Pharmaceuticals, Inc. EBIT Margin for the Trailing 12 Months (TTM) ending September 30, 2022 was 3.64%, a -85.04% change year over year.
  • Supernus Pharmaceuticals, Inc. EBIT Margin for the Trailing 12 Months (TTM) ending September 30, 2021 was 24.33%, a -33.05% change year over year.
  • Supernus Pharmaceuticals, Inc. EBIT Margin for the Trailing 12 Months (TTM) ending September 30, 2020 was 36.33%, a -8.22% change year over year.
Key data
Date EBIT Margin EPS (Basic) EPS (Diluted) Shares (Basic, Weighted)
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NasdaqGM: SUPN

Supernus Pharmaceuticals, Inc.

CEO Mr. Jack A. Khattar M.B.A.
IPO Date May 1, 2012
Location United States
Headquarters 9715 Key West Avenue
Employees 652
Sector Health Care
Industries
Description

Supernus Pharmaceuticals, Inc., a biopharmaceutical company, focuses on the development and commercialization of products for the treatment of central nervous system (CNS) diseases in the United States. Its commercial products are Trokendi XR, an extended release topiramate product indicated for the treatment of epilepsy, as well as for the prophylaxis of migraine headache; and Oxtellar XR, an extended release oxcarbazepine for the monotherapy treatment of partial onset epilepsy seizures in adults and children between 6 to 17 years of age. The company's commercial products also comprise Qelbree, a selective norepinephrine reuptake inhibitor indicated for the treatment of attention-deficit hyperactivity disorder (ADHD) in pediatric patients 6 to 17 years of age; APOKYN for the acute intermittent treatment of hypomobility or off episodes in patients with advanced Parkinson's Disease (PD); XADAGO for treating levodopa/carbidopa in patients with PD experiencing off episodes; MYOBLOC, a Type B toxin product indicated for the treatment of cervical dystonia and sialorrhea in adults; GOCOVRI for the treatment of dyskinesia in patients with PD; and Osmolex ER for the treatment of Parkinson's disease and drug-induced extrapyramidal reaction in adult patients. In addition, its product candidates include Qelbree (SPN-812), which has completed Phase III clinical trials that is used for the treatment of ADHD; SPN-830, a late-stage drug/device combination product candidate for the prevention of off episodes in PD patients; SPN-817, a novel product candidate in Phase I clinical trials for the treatment of severe epilepsy; SPN-820, a product candidate in Phase II clinical trials for treating resistant depression; and SPN-443 and SPN-446, which are in preclinical stage for treating CNS. The company markets and sells its products through pharmaceutical wholesalers, specialty pharmacies, and distributors. The company was incorporated in 2005 and is headquartered in Rockville, Maryland.

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StockViz Staff

January 15, 2025

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