Sunosi Generic: When Will Generic Solriamfetol Be Available?

Dr. Brian Staiger, PharmD, BCPS

This page is aggregated from FDA records, court filings and company announcements. Coded and designed by

Updated October 9, 2026 How we build our data

Sunosi Generic at a Glance

Four quick answers from FDA records and our estimate.

  1. When is the first generic expected? During 2040 Sometime that year Why then?
  2. Has the FDA approved a generic? June 2026 2 companies approved Why not on sale?
  3. When does the last patent end? December 2042 42 patents listed with the FDA Why is a generic expected sooner?
  4. Can you buy a generic today? Not yet No company lists one for sale

Explains

PharmD, BCPS · Clinical pharmacist Updated

Generic solriamfetol hydrochloride is expected to be available sometime in 2040. None is for sale yet.

Why 2040?

The brand company and a generic maker settled their patent fight and agreed on when a generic can launch. We rate it probable: more likely than not, but it can still move.

If Sunosi’s last patent runs to December 2042, how can a generic come sooner?

The 12 patents that run past the expected month, to December 2042 (11,771,666, 11,771,667, 11,779,554, 11,793,776 and 8 more), cover a way of using it. A patent like that protects one way of making or using the medicine, not the medicine itself. A generic company can often make its version a different way or leave that use off its label, or a court can rule the patent invalid or not infringed. Here, a settlement between the companies sets the date. Generic companies have been challenging Sunosi’s patents with the FDA since June 2023. That is why the expected month comes before the last protection ends. See the road to a generic

If the FDA approved a generic, why can’t I buy one?

FDA approval is permission to sell, not a launch. 2 companies have held approvals since June 2026, but a patent, a settlement or a company’s own plans can hold a generic back until the expected month. See who is lined up

Will the generic cost less?

Usually, and more so as more companies sell one. 6 companies have applied to the FDA to make it. In the FDA’s study of past launches, pharmacies paid over 95% less once six or more companies sold a generic, which would take the $31.37 pharmacies pay per tablet for Sunosi today to under $1.57. See the price estimate

What should I do now?

Keep taking Sunosi as prescribed. When a generic arrives, your pharmacy may switch you to it automatically, and it may look different. What a generic means for you

Our month is only an estimate based on available information, so we never name a day.

Sunosi by the Numbers

Reason
Settlement between companiesThe brand company and a generic maker settled their patent fight and agreed on when a generic can launch.
How sure
Probable More likely than not, but it can still move.
Price competition
Very strong 6 companies have filed, 6 first in line
Brand sales
$206M a yearBig seller
  • FDA approved 2019 June 2019 FDA Orange Book
  • Patents listed 42 last runs to December 2042 A generic is expected sooner, sometime in 2040. See why FDA Orange Book
  • Generics FDA-approved 2 companies, the first approved June 2026 FDA Orange Book
  • Pharmacies pay $31.37 per tablet, up 12.9% in a year NADAC, October 2026
  • Medicare Part D spent $26.4M in 2025, for 4,443 people CMS Part D Spending by Drug
  • Medicaid prescriptions 15.6K in the last four reported quarters, $14.5M CMS Medicaid drug utilization, to Q1 2026

Sunosi’s Road to a Generic

Sunosi has had the market to itself since the FDA approved it in June 2019 (Axsome Malta Ltd). Its FDA protections on record ended by June 2026. Its 42 listed patents run to December 2042 (5 already expired). Generic companies have challenged its patents with the FDA since June 2023.

The first generic of Sunosi is expected sometime in 2040.

Why that month: the brand company and a generic maker settled their patent fight and agreed on when a generic can launch.

Brand alone on the market Since FDA approval, June 2019
Orphan drug Ended June 2026
Patent 11,771,666 Expires December 2042
Patent 11,771,667 Expires December 2042
Patent 11,779,554 Expires December 2042
Patent 11,793,776 Expires December 2042
Patent 11,872,203 Expires December 2042
Patent 11,872,204 Expires December 2042
Brand alone on the market FDA exclusivity Patent on a use First generic expected 36 more patents end earlier; every patent is in the table below. Swipe the chart sideways to see every year.

Why a Generic Can Come Before December 2042

The last listed patent runs to December 2042, but it covers a way of using it, not the medicine itself, which a generic can often work around or challenge. Dr. Brian explains

Each bar runs from the brand’s approval to the day that protection ends. The green band is our projection for the first generic: a month, never a day, because legal dates move and a generic reaches shelves days to weeks after it is allowed. Sources: FDA Orange Book; the expected month from court records and company announcements.

Sunosi Patents and FDA Protections

Every patent and exclusivity the FDA Orange Book lists for Sunosi’s own applications. A protection running past the expected month does not mean the date is wrong: a settlement or a court ruling can let a generic in before a patent ends, and a patent on one formulation or use does not block every generic.

Patents listed with the FDA (42)
PatentWhat it coversProtects untilStatus
8,877,806 A way of using it (U-2548) June 2026 Expired
9,604,917 A way of using it (U-2548) June 2026 Expired
10,351,517 A way of using it (U-2548) June 2026 Expired
11,753,368 A way of using it (U-2548) June 2026 Expired
12,209,059 A way of using it (U-2548) June 2026 Expired
8,440,715 A way of using it (U-2548) June 2031 Active
10,195,151 The product’s formulation September 2037 Active
10,512,609 A way of using it (U-2548) September 2037 Active
11,439,597 The product’s formulation September 2037 Active
11,998,639 The product’s formulation; a way of using it (U-2548) September 2037 Active
12,390,419 The product’s formulation; a way of using it (U-2548) September 2037 Active
10,912,754 A way of using it (U-3082) June 2038 Active
10,959,976 A way of using it (U-3151) June 2038 Active
11,648,232 A way of using it (U-3602) June 2038 Active
11,865,098 A way of using it (U-2548) June 2038 Active
12,384,743 The active ingredient; the product’s formulation; a way of using it (U-2548) November 2038 Active
11,560,354 The product’s formulation; a way of using it (U-3520) March 2039 Active
10,940,133 A way of using it (U-3099) March 2040 Active
11,160,779 A way of using it (U-3521) March 2040 Active
11,839,598 A way of using it (U-3765) March 2040 Active
11,839,599 A way of using it (U-3764) March 2040 Active
11,850,226 A way of using it (U-3775) March 2040 Active
11,850,227 A way of using it (U-3775) March 2040 Active
11,850,228 A way of using it (U-3775) March 2040 Active
11,857,528 A way of using it (U-3521) March 2040 Active
11,969,404 A way of using it (U-3892) March 2040 Active
11,986,454 A way of using it (U-3775) March 2040 Active
11,986,455 A way of using it (U-3521) March 2040 Active
12,194,016 A way of using it (U-4106) March 2040 Active
12,318,362 A way of using it (U-3765) March 2040 Active
11,771,666 A way of using it (U-3693) December 2042 Active
11,771,667 A way of using it (U-3693) December 2042 Active
11,779,554 A way of using it (U-3693) December 2042 Active
11,793,776 A way of using it (U-3693) December 2042 Active
11,872,203 A way of using it (U-3693) December 2042 Active
11,872,204 A way of using it (U-3693) December 2042 Active
12,005,036 A way of using it (U-3693) December 2042 Active
12,036,194 A way of using it (U-3693) December 2042 Active
12,064,411 A way of using it (U-3693) December 2042 Active
12,090,126 A way of using it (U-3693) December 2042 Active
12,102,609 A way of using it (U-3693) December 2042 Active
12,263,145 A way of using it (U-3693) December 2042 Active
FDA exclusivities (1)
ExclusivityWhat it meansEndsStatus
Orphan drug ODE-254Seven years of protection for a use in a rare disease.June 2026Ended

Source: FDA Orange Book, application 211230. Patent numbers open the patent on Google Patents.

Patent Challenges to Sunosi

The first patent challenge to Sunosi reached the FDA in June 2023, from 6 companies on that first day. The FDA approved a first challenger’s generic in June 2026, and the list records no sale by a first challenger yet.

What Is a Patent Challenge?

A generic company that wants to sell its version before Sunosi’s patents run out can tell the FDA that a patent is invalid, or that its version does not infringe it. The FDA calls this a “Paragraph IV certification.” The brand company usually sues, and the FDA then generally cannot approve that generic for up to 30 months while the case runs. To reward going first, the companies that challenge first can get a 180-day head start: the FDA cannot approve the generics that came after them until it ends.

Patent challenges on the FDA’s list (1)
ProductFirst challengedCompanies that day180-day head startFirst challenger’s genericChallenged patents run to
ApprovedOn sale
Tablets, 75 mg and 150 mg June 2023 6 companies First challenger eligible decided June 2026 June 2026 Not yet March 2040

Source: the FDA’s Paragraph IV Patent Certifications list, as of September 2026. The FDA began posting the 180-day decisions and the first challenger’s approval and first sale in June 2019: an older entry it has not updated since reads “Not posted”, and “Not yet” means the list records no such event. “Companies that day” is the FDA’s count of challenges that arrived on the first day.

Who Is Lined Up to Make Generic Solriamfetol Hydrochloride

Three steps stand between a brand and a generic you can buy: a company applies to the FDA, the FDA approves it, and the company starts selling it.

1

Applied to the FDA

6 companies have applied to the FDA to make generic solriamfetol hydrochloride.

The FDA keeps the other applications private until it acts on them, so those companies are not named here.

First in line. 6 of them were first in line, all filing on the first day any company did: they can share 180 days on the market before the other generics, which is why being first matters.

Generic companies have challenged Sunosi’s patents with the FDA since June 2023: see the patent challenges.

2

Approved by the FDA

The FDA has approved generic versions from 2 companies, the first in June 2026. Approved is not the same as on sale: patents, a settlement or the company’s own plans can still hold a launch.

3

For Sale in Pharmacies

Not yet. No company lists a generic solriamfetol hydrochloride for sale with the FDA.

Generic versions the FDA has approved (2 companies)
CompanyFirst approvedStrengthsRated
Alkem Laboratories Ltd June 2026EQ 75MG BASE, EQ 150MG BASEAB
Hikma Pharmaceuticals USA Inc June 2026EQ 75MG BASE, EQ 150MG BASEAB

Sources: how many companies have applied, from court records and company announcements; approved generics from the FDA Orange Book; tentative approvals from Drugs@FDA; what is for sale from the FDA NDC Directory. The FDA does not disclose an application before it approves it (21 CFR 314.430).

Sunosi Price: What Pharmacies Pay and What Generics Usually Do

What Pharmacies Pay for Sunosi 75 mg tablet

$31.37 per tablet in October 2026, up 12.9% from a year earlier.

Hover over or tap anywhere on the chart to see that month’s price.

  • Sunosi 75 mg tablet $31.37 per tablet
  • Sunosi 150 mg tablet $31.34 per tablet
See the numbers
MonthPharmacies paid per tablet
October 2026$31.37
September 2026$31.37
August 2026$31.38
July 2026$31.36
June 2026$31.33
May 2026$31.24
April 2026$31.22
March 2026$31.22
February 2026$31.22
January 2026$31.22
February 2024$27.79
January 2024$27.79

NADAC: the national average price retail pharmacies pay to buy the medicine (CMS survey, updated weekly), the last price of each month for one package. It is not what you pay: that depends on your insurance or discount card.

What a Generic Could Cost

What Pharmacies Pay for Sunosi Today$31.37per tablet · October 2026
Our Estimate for Generic Sunosiunder $1.57per tablet once generics reach pharmacies, over 95% less than today

How we estimate it. We start from what pharmacies pay for Sunosi today: $31.37 per tablet for Sunosi 75 mg tablet in October 2026, from the national NADAC survey. Then we apply the FDA’s finding of how far that price usually falls as generic companies join: about 31% with one company, 44% with two, 73% with four and over 95% with six or more (the typical drop for every drug whose first generic came out from 2015 to 2017). Sunosi has 6 companies lined up, so our estimate uses the figure for six or more companies. More companies would bring the price lower; fewer, less of a drop.

Dollar figures apply FDA’s median drops to the $31.37 pharmacies pay per tablet today. An estimate from the pattern, not a price quote: what you pay depends on your insurance or discount card.

Median prices pharmacies paid for the generic (invoice prices), compared with the brand’s price before generic entry, from FDA’s 2019 analysis “Generic Competition and Drug Prices”. At the manufacturer’s price FDA found steeper drops (about 39%, 54%, 79% and over 95%), the figures quoted elsewhere on this tracker. A typical pattern, not a price quote for this medicine.

What Medicare and Medicaid Spend on Sunosi

Big public spending is part of why generic makers line up for a medicine, and why its first generic matters beyond the pharmacy counter. Figures are before manufacturer rebates, which are confidential.

Medicare Part D Spending

What Medicare drug plans spent on Sunosi, before manufacturer rebates.

$6.8M
January to March 2026, the latest CMS has posted
For 2,897 people, about $1,171 per prescription fill
$26.4M
2025, the whole year
For 4,443 people, about $1,107 per prescription fill
See the numbers
PeriodSpendingPeoplePer fill
January to March 2026$6,754,1752,897$1,170.97
2025$26,353,3104,443$1,107.37

Source: CMS Medicare Part D Spending by Drug, matched by the brand name Sunosi only, so no generic is counted in it. What CMS says it is used for: This medication is used to improve wakefulness in people that have too much daytime sleepiness due to certain sleep problems (narcolepsy, obstructive sleep apnea). It may work by changing the amounts of certain substances (dopamine, norepinephrine) in your body.

Medicaid Prescriptions by Quarter

15,562 prescriptions in the four quarters to Q1 2026, $14.5M paid.

See the numbers
QuarterPrescriptionsMedicaid paid
Q1 20263,658$3,547,751
Q4 20254,020$3,689,579
Q3 20254,026$3,698,017
Q2 20253,858$3,553,845
Q1 20253,563$3,255,792

Source: CMS Medicaid State Drug Utilization Data, over Sunosi’s own package codes.

Sunosi Strengths and Forms

StrengthFormHow it is takenApprovedStatus
EQ 150MG BASETabletOralJune 2019Prescription reference product
EQ 75MG BASETabletOralJune 2019Prescription reference product

Source: FDA Orange Book, Axsome Malta Ltd. Listed for sale today by Jazz Pharmaceuticals, Inc. and Axsome Therapeutics, Inc. (FDA NDC Directory).

Sunosi NDC Codes and Packages

Each Sunosi package sold today has its own NDC, the product number printed on the box and on the pharmacy label. Open one to see that package’s details, what pharmacies pay for it and its patent timeline.

Sunosi packages (20)
NDCProductPackageCompany
68727-0350-0175 mg tablet, film coatedbottle of 30 tabletsJazz Pharmaceuticals, Inc.
68727-0350-0275 mg tablet, film coatedbottle of 100 tabletsJazz Pharmaceuticals, Inc.
68727-0350-0775 mg tablet, film coatedblister pack of 7 tabletsJazz Pharmaceuticals, Inc.
68727-0350-1075 mg tablet, film coatedcarton of 10 tabletsJazz Pharmaceuticals, Inc.
68727-0351-01150 mg tablet, film coatedbottle of 30 tabletsJazz Pharmaceuticals, Inc.
68727-0351-02150 mg tablet, film coatedbottle of 100 tabletsJazz Pharmaceuticals, Inc.
68727-0351-07150 mg tablet, film coatedblister pack of 7 tabletsJazz Pharmaceuticals, Inc.
68727-0351-10150 mg tablet, film coatedcarton of 10 tabletsJazz Pharmaceuticals, Inc.
Show the other 12 Sunosi packages
NDCProductPackageCompany
81968-0351-01SOLRIAMFETOL 150 mg/1 tablet, film coatedbottle of 30 tabletsAxsome Therapeutics, Inc.
81968-0351-01SOLRIAMFETOL 150 mg/1 tablet, film coatedbottle of 30 tabletsAxsome Therapeutics, Inc.
81968-0351-07SOLRIAMFETOL 150 mg/1 tablet, film coatedblister pack of 7 tabletsAxsome Therapeutics, Inc.
81968-0351-07SOLRIAMFETOL 150 mg/1 tablet, film coatedblister pack of 7 tabletsAxsome Therapeutics, Inc.
81968-0351-10SOLRIAMFETOL 150 mg/1 tablet, film coatedcarton of 10 blister packs of 7 tabletsAxsome Therapeutics, Inc.
81968-0351-10SOLRIAMFETOL 150 mg/1 tablet, film coatedcarton of 10 blister packs of 7 tabletsAxsome Therapeutics, Inc.
81968-0350-01SOLRIAMFETOL 75 mg/1 tablet, film coatedbottle of 30 tabletsAxsome Therapeutics, Inc.
81968-0350-01SOLRIAMFETOL 75 mg/1 tablet, film coatedbottle of 30 tabletsAxsome Therapeutics, Inc.
81968-0350-07SOLRIAMFETOL 75 mg/1 tablet, film coatedblister pack of 7 tabletsAxsome Therapeutics, Inc.
81968-0350-07SOLRIAMFETOL 75 mg/1 tablet, film coatedblister pack of 7 tabletsAxsome Therapeutics, Inc.
81968-0350-10SOLRIAMFETOL 75 mg/1 tablet, film coatedcarton of 10 blister packs of 7 tabletsAxsome Therapeutics, Inc.
81968-0350-10SOLRIAMFETOL 75 mg/1 tablet, film coatedcarton of 10 blister packs of 7 tabletsAxsome Therapeutics, Inc.

Source: the FDA NDC Directory, current listings only. Only packages sold under Sunosi’s own FDA approval (NDA 211230) are listed, never a generic. Some codes belong to companies that repackage Sunosi: it is the same medicine in a different package.

What a Generic Sunosi Means for You

Nothing Changes Until It Is in Pharmacies

Until a generic is actually for sale, keep filling Sunosi as usual. When one arrives, there is nothing you need to sign up for.

Your Pharmacy May Switch You Automatically

Every state lets pharmacists fill a brand-name prescription with an FDA-approved generic rated as equivalent to it, and about 19 states require them to, unless your prescriber writes “dispense as written” or “brand medically necessary” on the prescription. Some states ask the pharmacist to tell you, or to get your OK first. A study of every state’s law has the details.

It Will Probably Look Different

US trademark law does not let a generic look exactly like the brand, so the color, shape or markings usually change. The active ingredient, strength and form are the same. An “authorized generic,” made by or for the brand’s own company, can look identical. The FDA explains.

Your Insurance May Change Too

Once a lower-cost version is available, many insurance plans charge more for the brand, or stop covering it. Your plan’s drug list (formulary) says how.

Until a generic is on US pharmacy shelves, be careful with websites that offer “generic Sunosi”. The FDA warns that unlicensed online pharmacies sell counterfeit and unapproved medicines; its BeSafeRx page shows how to check a pharmacy.

Questions people ask about Sunosi

Is there a generic for Sunosi right now?

No. As of October 9, 2026 no generic solriamfetol hydrochloride is listed for sale in the FDA NDC Directory. 2 generic versions are FDA-approved (Orange Book), which usually means it is waiting on patents or on the maker’s own launch plans.

When will Sunosi go generic?

Sometime in 2040 is the expected window, and that is probable but not certain. The brand company and a generic maker settled their patent fight and agreed on when a generic can launch. The last listed patent runs to December 2042, but it covers a way of using it, not the medicine itself, which a generic can often work around or challenge.

Will generic solriamfetol hydrochloride be the same as Sunosi?

Yes in the ways that matter: the same active ingredient, strength and form, with proof that it reaches your blood the same way. Inactive ingredients can differ, which is why some people notice a different look or taste.

How much will the generic cost?

Nobody can say for sure before launch. 6 companies have applied to the FDA to make it. In the FDA’s study of past launches, pharmacies paid over 95% less once six or more companies sold a generic, which would take the $31.37 pharmacies pay per tablet for Sunosi today to under $1.57. That is a pattern from past launches, not a prediction for this one.

Has the FDA approved a generic Sunosi?

Yes. The FDA Orange Book lists approved generic versions from 2 companies, the first approved in June 2026: Alkem Laboratories Ltd and Hikma Pharmaceuticals USA Inc. Approved is not the same as on sale: patents, a settlement or the company’s own plans can still hold a launch.

When does the Sunosi patent expire?

The FDA Orange Book lists 42 patents for Sunosi; the last runs to December 2042. A patent date is not the launch date: settlements and court rulings often bring a generic earlier, and FDA approval or a company’s own plans can make it later. The expected window on this page (Sometime in 2040) weighs all of that.

Has anyone challenged the Sunosi patents?

Yes. The first patent challenge to Sunosi reached the FDA in June 2023, from 6 companies on that first day. The FDA approved a first challenger’s generic in June 2026, and the list records no sale by a first challenger yet. A patent challenge (a “Paragraph IV certification”) is a generic company telling the FDA that a patent listed for the brand is invalid or will not be infringed by its version. The first companies to file one can earn a 180-day head start, during which the FDA cannot approve the generics that filed after them.

How much does Sunosi cost now?

Pharmacies paid about $31.37 per tablet for Sunosi 75 mg tablet in October 2026, by the national survey of what pharmacies pay (NADAC). That is the pharmacy’s cost, not your price: what you pay depends on your insurance or discount card.

Changes to This Projection

  • First generic expected Sometime in 2040 on this month’s schedule. A line is added here whenever a monthly update moves the month, the reason or how sure it is.

Every change to the expected month is logged here with the month we saw it.

Also Going Generic

All upcoming generics

About Sunosi

Sources. The expected month: FDA Paragraph IV Patent Certifications list, federal court records, company announcements and securities filings (settlement dates, launch plans, sales). The record on this page: FDA Orange Book, Drugs@FDA (tentative approvals), FDA NDC Directory, FDA Paragraph IV Patent Certifications list, NADAC (CMS), CMS Medicare Part D Spending by Drug, Medicaid State Drug Utilization Data, FDA, Generic Competition and Drug Prices (2019). Updated October 9, 2026. Information, not medical advice.