Seysara Generic: When Will Generic Sarecycline 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

Seysara Generic at a Glance

Four quick answers from FDA records and our estimate.

  1. When is the first generic expected? February 2033 About 6.5 years away Why then?
  2. Has the FDA approved a generic? Not yet None in the FDA’s records yet Why not yet?
  3. When does the last patent end? February 2033 4 patents listed with the FDA
  4. Can you buy a generic today? Not yet No company lists one for sale

Explains

PharmD, BCPS · Clinical pharmacist Updated

Generic sarecycline hydrochloride is expected to be available in February 2033, about 6.5 years away. None is for sale yet.

Why February 2033?

It is when Seysara’s patent 9,255,068 ends. That patent covers the active ingredient, the product’s formulation and a way of using it, and once it ends, generics can go on sale as soon as the FDA approves them. We rate it probable: more likely than not, but it can still move.

Why hasn’t the FDA approved a generic yet?

That is normal before a launch. The FDA usually can’t give a generic its final approval while a patent or exclusivity still blocks it, so final approval often comes close to the day the generic can be sold. A company may already hold a “tentative” approval, which this record does not show.

Will the generic cost less?

Usually, but no company is recorded as having applied to make one yet, and a single company usually brings only a modest drop. See the price pattern

What should I do now?

Keep taking Seysara 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.

Seysara by the Numbers

Reason
Patent expiresA patent that protects the brand runs out. After that, approved generics can be sold.
How sure
Probable More likely than not, but it can still move.
Price competition
None filed yet No filers on record
Brand sales
$58M a yearSmaller seller
  • FDA approved 2018 October 2018 FDA Orange Book
  • Patents listed 4 last runs to February 2033 FDA Orange Book
  • Medicare Part D spent $849.2K in 2025, for 193 people CMS Part D Spending by Drug

Seysara’s Road to a Generic

Seysara has had the market to itself since the FDA approved it in October 2018 (Almirall LLC). Its 4 listed patents run to February 2033.

The first generic of Seysara is expected in February 2033.

Why that month: patent 9,255,068, on the active ingredient, the product’s formulation and a way of using it, ends then.

Brand alone on the market Since FDA approval, October 2018
Patent 9,481,639 Expires August 2028
Patent 8,513,223 Expires December 2029
Patent 8,318,706 Expires January 2032
Patent 9,255,068 Expires February 2033 The patent behind the expected month of generic availability
Brand alone on the market Patent on the active ingredient Patent on a use First generic expected Swipe the chart sideways to see every year.

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.

Seysara Patents and FDA Protections

Every patent and exclusivity the FDA Orange Book lists for Seysara’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.

The one that matters for a generic launch: patent 9,255,068, which ends in February 2033, the month the first generic is expected.

Patents listed with the FDA (4)
PatentWhat it coversProtects untilStatus
9,481,639 A way of using it (U-2409) August 2028 Active
8,513,223 A way of using it (U-2406) December 2029 Active
8,318,706 The active ingredient; the product’s formulation; a way of using it (U-2405) January 2032 Active
9,255,068 Sets the expected month of generic availability The active ingredient; the product’s formulation; a way of using it (U-2407, U-2408) February 2033 Active

Source: FDA Orange Book, application 209521. Patent numbers open the patent on Google Patents.

Who Is Lined Up to Make Generic Sarecycline 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

No company is recorded as having applied to the FDA to make a generic Seysara yet.

2

Approved by the FDA

Not yet. The FDA has not approved a generic sarecycline hydrochloride. Final approval often comes close to the day a generic can be sold.

3

For Sale in Pharmacies

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

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

Seysara Price: What Pharmacies Pay and What Generics Usually Do

What a Generic Could Cost

How we estimate it. The national survey of what pharmacies pay (NADAC) has no recent price for Seysara, so we cannot show dollars. Here is the FDA’s finding of how far the price pharmacies pay 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).

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 Seysara

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 Seysara, before manufacturer rebates.

$223.1K
January to March 2026, the latest CMS has posted
For 102 people, about $1,289 per prescription fill
$849.2K
2025, the whole year
For 193 people, about $1,249 per prescription fill
See the numbers
PeriodSpendingPeoplePer fill
January to March 2026$223,053102$1,289.33
2025$849,232193$1,248.87

Source: CMS Medicare Part D Spending by Drug, matched by the brand name Seysara only, so no generic is counted in it. What CMS says it is used for: Sarecycline is used to treat moderate to severe acne. This medication belongs to a class of drugs known as tetracycline antibiotics.

Seysara Strengths and Forms

StrengthFormHow it is takenApprovedStatus
EQ 100MG BASETabletOralOctober 2018Prescription reference product
EQ 150MG BASETabletOralOctober 2018Prescription reference product
EQ 60MG BASETabletOralOctober 2018Prescription reference product

Source: FDA Orange Book, Almirall LLC. Listed for sale today by Almirall, LLC (FDA NDC Directory).

Seysara NDC Codes and Packages

Each Seysara 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.

Seysara packages (9)
NDCProductPackageCompany
16110-0246-00SARECYCLINE HYDROCHLORIDE 100 mg/1 tablet, coatedbag of 29,000 tabletsAlmirall, LLC
16110-0246-30SARECYCLINE HYDROCHLORIDE 100 mg/1 tablet, coatedbottle of 30 tabletsAlmirall, LLC
16110-0246-30SARECYCLINE HYDROCHLORIDE 100 mg/1 tablet, coatedbottle of 30 tabletsAlmirall, LLC
16110-0247-00SARECYCLINE HYDROCHLORIDE 150 mg/1 tablet, coatedbag of 192,000 tabletsAlmirall, LLC
16110-0247-30SARECYCLINE HYDROCHLORIDE 150 mg/1 tablet, coatedbottle of 30 tabletsAlmirall, LLC
16110-0247-30SARECYCLINE HYDROCHLORIDE 150 mg/1 tablet, coatedbottle of 30 tabletsAlmirall, LLC
16110-0245-00SARECYCLINE HYDROCHLORIDE 60 mg/1 tablet, coatedbag of 48,000 tabletsAlmirall, LLC
16110-0245-30SARECYCLINE HYDROCHLORIDE 60 mg/1 tablet, coatedbottle of 30 tabletsAlmirall, LLC
16110-0245-30SARECYCLINE HYDROCHLORIDE 60 mg/1 tablet, coatedbottle of 30 tabletsAlmirall, LLC

Source: the FDA NDC Directory, current listings only. Only packages sold under Seysara’s own FDA approval (NDA 209521) are listed, never a generic. Some codes belong to companies that repackage Seysara: it is the same medicine in a different package.

What a Generic Seysara Means for You

Nothing Changes Until It Is in Pharmacies

Until a generic is actually for sale, keep filling Seysara 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 Seysara”. 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 Seysara

Is there a generic for Seysara right now?

No. As of October 9, 2026 no generic sarecycline hydrochloride is listed for sale in the FDA NDC Directory.

When will Seysara go generic?

February 2033 is the expected month, and that is probable but not certain. It is when Seysara’s patent 9,255,068 ends. That patent covers the active ingredient, the product’s formulation and a way of using it, and once it ends, generics can go on sale as soon as the FDA approves them.

Will generic sarecycline hydrochloride be the same as Seysara?

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. No company is recorded as having applied to the FDA to make one yet, and a single company usually brings only a modest drop.

Has the FDA approved a generic Seysara?

Not yet. The FDA Orange Book lists no approved generic version of Seysara.

When does the Seysara patent expire?

The FDA Orange Book lists 4 patents for Seysara; the last runs to February 2033. The one behind the expected month is patent 9,255,068, which ends in February 2033. 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 month on this page (February 2033) weighs all of that.

Changes to This Projection

  • First generic expected February 2033 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 Seysara

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, FDA NDC Directory, CMS Medicare Part D Spending by Drug, FDA, Generic Competition and Drug Prices (2019). Updated October 9, 2026. Information, not medical advice.