Synribo Generic: When Will Generic Omacetaxine Mepesuccinate Be Available?
This page is aggregated from FDA records, court filings and company announcements. Coded and designed by Dr. Brian Staiger, PharmD, BCPS
Updated October 9, 2026 How we build our data
Synribo Generic at a Glance
Four quick answers from FDA records and our estimate.
- When is the first generic expected? October 2026 This month Why then?
- Has the FDA approved a generic? Not yet None in the FDA’s records yet Why not yet?
- When does the last patent end? October 2026 Its only patent listed with the FDA
- Can you buy a generic today? Not yet No company lists one for sale
Generic omacetaxine mepesuccinate is expected to be available in October 2026, this month. None is for sale yet.
Why October 2026?
It is when Synribo’s patent 6,987,103 ends. That patent covers a way of using it, and once it ends, generics can go on sale as soon as the FDA approves them. We rate it toss-up: still unsettled. Just as likely to slip as to hold.
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, and more so as more companies sell one. One company has applied to the FDA to make it. In the FDA’s study of past launches, pharmacies paid about 31% less once one company sold a generic. See the price pattern
What should I do now?
Keep taking Synribo 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.
Synribo by the Numbers
- Reason
- Patent expiresA patent that protects the brand runs out. After that, approved generics can be sold.
- How sure
- Toss-up Still unsettled. Just as likely to slip as to hold.
- Price competition
- Low 1 company has filed
- Brand sales
- Sales not reported
- FDA approved 2012 October 2012 FDA Orange Book
- Patents listed 1 last runs to October 2026 FDA Orange Book
Synribo’s Road to a Generic
Synribo has had the market to itself since the FDA approved it in October 2012 (Teva Pharmaceuticals International GmbH). Its one listed patent runs to October 2026. Generic companies have challenged its patents with the FDA since October 2016.
The first generic of Synribo is expected in October 2026.
Why that month: patent 6,987,103, on a way of using it, ends then.
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.
Synribo Patents and FDA Protections
Every patent and exclusivity the FDA Orange Book lists for Synribo’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 6,987,103, which ends in October 2026, the month the first generic is expected.
| Patent | What it covers | Protects until | Status |
|---|---|---|---|
| 6,987,103 Sets the expected month of generic availability | A way of using it (U-1300) | October 2026 | Active |
Source: FDA Orange Book, application 203585. Patent numbers open the patent on Google Patents.
Patent Challenges to Synribo
The first patent challenge to Synribo reached the FDA in October 2016, from one company on that first day. The FDA has not approved a first challenger’s generic yet.
What Is a Patent Challenge?
A generic company that wants to sell its version before Synribo’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.
| Product | First challenged | Companies that day | 180-day head start | First challenger’s generic | Challenged patents run to | |
|---|---|---|---|---|---|---|
| Approved | On sale | |||||
| For injection, 3.5 mg/vial | October 2016 | 1 company | Head start no longer applies decided February 2022 | Not yet | Not yet | June 2023 |
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 Omacetaxine Mepesuccinate
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.
Applied to the FDA
One company has applied to the FDA to make generic omacetaxine mepesuccinate.
The FDA names a company only once it approves its application, even tentatively, and it has not done that for this one yet, so the company is not named here. Names often come out in the brand company’s patent lawsuits or in the companies’ own announcements.
Generic companies have challenged Synribo’s patents with the FDA since October 2016: see the patent challenges.
Approved by the FDA
Not yet. The FDA has not approved a generic omacetaxine mepesuccinate. Final approval often comes close to the day a generic can be sold.
For Sale in Pharmacies
Not yet. No company lists a generic omacetaxine mepesuccinate 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).
Synribo 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 Synribo, 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.
Synribo Strengths and Forms
| Strength | Form | How it is taken | Approved | Status |
|---|---|---|---|---|
| 3.5MG/VIAL | Powder | Subcutaneous | October 2012 | Discontinued reference product |
Source: FDA Orange Book, Teva Pharmaceuticals International GmbH. Listed for sale today by Cephalon, LLC (FDA NDC Directory).
Synribo NDC Codes and Packages
Each Synribo 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.
| NDC | Product | Package | Company |
|---|---|---|---|
| 63459-0177-14 | 3.5 mg/mL injection, powder, lyophilized, for solution | vial of 1 mL | Cephalon, LLC |
Source: the FDA NDC Directory, current listings only. Only packages sold under Synribo’s own FDA approval (NDA 203585) are listed, never a generic. Some codes belong to companies that repackage Synribo: it is the same medicine in a different package.
What a Generic Synribo Means for You
Nothing Changes Until It Is in Pharmacies
Until a generic is actually for sale, keep filling Synribo 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 Synribo”. 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 Synribo
Is there a generic for Synribo right now?
No. As of October 9, 2026 no generic omacetaxine mepesuccinate is listed for sale in the FDA NDC Directory.
When will Synribo go generic?
October 2026 is the expected month, and that is toss-up but not certain. It is when Synribo’s patent 6,987,103 ends. That patent covers a way of using it, and once it ends, generics can go on sale as soon as the FDA approves them.
Will generic omacetaxine mepesuccinate be the same as Synribo?
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. One company has applied to the FDA to make it. In the FDA’s study of past launches, pharmacies paid about 31% less once one company sold a generic. That is a pattern from past launches, not a prediction for this one.
Has the FDA approved a generic Synribo?
Not yet. The FDA Orange Book lists no approved generic version of Synribo.
When does the Synribo patent expire?
One patent is listed for Synribo in the FDA Orange Book; it runs to October 2026. The one behind the expected month is patent 6,987,103, which ends in October 2026. 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 (October 2026) weighs all of that.
Has anyone challenged the Synribo patents?
Yes. The first patent challenge to Synribo reached the FDA in October 2016, from one company on that first day. The FDA has not approved a first challenger’s generic 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.
Changes to This Projection
- First generic expected October 2026 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
- AdempasRiociguatOctober to December 2026
- VarubiRolapitant HydrochlorideAugust 2028
- ImcivreeSetmelanotide AcetateJuly 2034
- RinvoqUpadacitinibApril 2037
- Daybue StixTrofinetide2038 to 2039
- NeuproRotigotineTBD no date yet
About Synribo
- Generic name omacetaxine mepesuccinate
- How it is taken Injection under the skin
- Company Teva Pharmaceuticals International GmbH
- Patent challenges Since October 2016 (FDA)
- More drugs Brand-name drugs starting with S
- Have a question? A pharmacist answers, free. Ask about Synribo
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, FDA, Generic Competition and Drug Prices (2019). Updated October 9, 2026. Information, not medical advice.