Sezaby Generic: When Will Generic Phenobarbital 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

Sezaby Generic at a Glance

Four quick answers from FDA records and our estimate.

  1. When is the first generic expected? November 2029 About 3 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? April 2042 2 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 phenobarbital sodium is expected to be available in November 2029, about 3 years away. None is for sale yet.

Why November 2029?

It is when Sezaby’s FDA protection for orphan drug ends. Seven years of protection for a use in a rare disease. We rate it probable: more likely than not, but it can still move.

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

The 2 patents that run past the expected month, to April 2042 (11,857,683 and 12,636,254), cover the product’s formulation and 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. That is why the expected month comes before the last protection ends. See the road to a generic

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. No company holds a “tentative” approval yet either (the FDA’s word for a generic that is ready but still blocked).

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 Sezaby 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.

Sezaby by the Numbers

Reason
FDA exclusivity endsFDA gives new drugs a protected period, for example for a rare-disease use. It ends then.
How sure
Probable More likely than not, but it can still move.
Price competition
None filed yet No filers on record
Brand sales
$1M a yearSmaller seller
  • FDA approved 2022 November 2022 FDA Orange Book
  • Patents listed 2 last runs to April 2042 A generic is expected sooner, in November 2029. See why FDA Orange Book

Sezaby’s Road to a Generic

Sezaby has had the market to itself since the FDA approved it in November 2022 (Sun Pharmaceutical Industries Inc). Its FDA protection (orphan drug) runs to November 2029. Its 2 listed patents run to April 2042.

The first generic of Sezaby is expected in November 2029.

Why that month: FDA gives new drugs a protected period, for example for a rare-disease use. It ends then. That is about 12.5 years before the last listed patent runs out, in April 2042.

Brand alone on the market Since FDA approval, November 2022
Orphan drug Ends November 2029 The protection behind the expected month of generic availability
Patent 11,857,683 Expires April 2042
Patent 12,636,254 Expires April 2042
Brand alone on the market FDA exclusivity Patent on the formulation First generic expected Swipe the chart sideways to see every year.

Why a Generic Can Come Before April 2042

The last listed patent runs to April 2042, but it covers the product’s formulation and 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.

Sezaby Patents and FDA Protections

Every patent and exclusivity the FDA Orange Book lists for Sezaby’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 (2)
PatentWhat it coversProtects untilStatus
11,857,683 The product’s formulation; a way of using it (U-3779) April 2042 Active
12,636,254 The product’s formulation; a way of using it (U-3779) April 2042 Active
FDA exclusivities (1)
ExclusivityWhat it meansEndsStatus
Orphan drug ODE-414Seven years of protection for a use in a rare disease.November 2029Active

Source: FDA Orange Book, application 215910. Patent numbers open the patent on Google Patents.

Who Is Lined Up to Make Generic Phenobarbital Sodium

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 Sezaby yet.

2

Approved by the FDA

Not yet. The FDA has not approved a generic phenobarbital sodium. 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 phenobarbital sodium for sale with the FDA.

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).

Sezaby 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 Sezaby, 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.

Sezaby Strengths and Forms

StrengthFormHow it is takenApprovedStatus
100MG/VIALPowderIntravenousNovember 2022Prescription reference product

Source: FDA Orange Book, Sun Pharmaceutical Industries Inc. Listed for sale today by Sun Pharmaceutical Industries, Inc. (FDA NDC Directory).

Sezaby NDC Codes and Packages

Each Sezaby 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.

Sezaby packages (2)
NDCProductPackageCompany
62756-0301-01PHENOBARBITAL SODIUM 100 mg/1 injectionvial of 1 injectionSun Pharmaceutical Industries, Inc.
62756-0301-01PHENOBARBITAL SODIUM 100 mg/1 injectionvial of 1 injectionSun Pharmaceutical Industries, Inc.

Source: the FDA NDC Directory, current listings only. Only packages sold under Sezaby’s own FDA approval (NDA 215910) are listed, never a generic. Some codes belong to companies that repackage Sezaby: it is the same medicine in a different package.

What a Generic Sezaby Means for You

Nothing Changes Until It Is in Pharmacies

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

Is there a generic for Sezaby right now?

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

When will Sezaby go generic?

November 2029 is the expected month, and that is probable but not certain. It is when Sezaby’s FDA protection for orphan drug ends. Seven years of protection for a use in a rare disease. The last listed patent runs to April 2042, but it covers the product’s formulation and a way of using it, not the medicine itself, which a generic can often work around or challenge.

Will generic phenobarbital sodium be the same as Sezaby?

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 Sezaby?

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

When does the Sezaby patent expire?

The FDA Orange Book lists 2 patents for Sezaby; the last runs to April 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 month on this page (November 2029) weighs all of that.

Changes to This Projection

  • First generic expected November 2029 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 Sezaby

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, Generic Competition and Drug Prices (2019). Updated October 9, 2026. Information, not medical advice.