Olumiant Generic: When Will Generic Baricitinib 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
Olumiant Generic at a Glance
Four quick answers from FDA records and our estimate.
- When is the first generic expected? January to June 2032 A 6-month window Why then?
- Has the FDA approved a generic? July 2024 1 company approved Why not on sale?
- When does the last patent end? November 2032 6 patents listed with the FDA Why is a generic expected sooner?
- Can you buy a generic today? Not yet No company lists one for sale
Generic baricitinib is expected to be available between January and June 2032. None is for sale yet.
Why January to June 2032?
The brand company and a generic maker settled their patent fight and agreed on when a generic can launch. We rate it likely: firm enough to plan around, but a court ruling or a new deal could still move it.
If Olumiant’s last patent runs to November 2032, how can a generic come sooner?
The 2 patents that run past the expected month, to November 2032 (9,089,574 and 11,045,474), 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 Olumiant’s patents with the FDA since May 2022. 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. One company has held an approval since July 2024, 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. 2 companies have applied to the FDA to make it. In the FDA’s study of past launches, pharmacies paid about 44% less once two companies sold a generic, which would take the $92.54 pharmacies pay per tablet for Olumiant today to about $51.82. See the price estimate
What should I do now?
Keep taking Olumiant 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.
Olumiant 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
- Likely Firm enough to plan around, but a court ruling or a new deal could still move it.
- Price competition
- Moderate 2 companies have filed, 2 first in line
- Brand sales
- $501M a yearBig seller
- FDA approved 2018 May 2018 FDA Orange Book
- Patents listed 6 last runs to November 2032 A generic is expected sooner, between January and June 2032. See why FDA Orange Book
- Generics FDA-approved 1 company, approved July 2024 FDA Orange Book
- Pharmacies pay $92.54 per tablet NADAC, October 2026
- Medicare Part D spent $48.4M in 2025, for 1,909 people CMS Part D Spending by Drug
- Medicaid prescriptions 5,747 in the last four reported quarters, $26.6M CMS Medicaid drug utilization, to Q1 2026
Olumiant’s Road to a Generic
Olumiant has had the market to itself since the FDA approved it in May 2018 (Eli Lilly And Co). Its 6 listed patents run to November 2032. Generic companies have challenged its patents with the FDA since May 2022.
The first generic of Olumiant is expected between January and June 2032.
Why that month: the brand company and a generic maker settled their patent fight and agreed on when a generic can launch.
Why a Generic Can Come Before November 2032
The last listed patent runs to November 2032, 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.
Olumiant Patents and FDA Protections
Every patent and exclusivity the FDA Orange Book lists for Olumiant’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.
| Patent | What it covers | Protects until | Status |
|---|---|---|---|
| 8,420,629 | A way of using it (U-247) | March 2029 | Active |
| 9,737,469 | A way of using it (U-3500) | November 2031 | Active |
| 11,806,555 | A way of using it (U-3500) | November 2031 | Active |
| 8,158,616 | The active ingredient; the product’s formulation | May 2032 | Active |
| 9,089,574 | A way of using it (U-3372) | November 2032 | Active |
| 11,045,474 | A way of using it (U-3372) | November 2032 | Active |
Source: FDA Orange Book, application 207924. Patent numbers open the patent on Google Patents.
Patent Challenges to Olumiant
The first patent challenge to Olumiant reached the FDA in May 2022, from 2 companies on that first day. The FDA’s list has 2 entries for Olumiant, by form and strength. The FDA approved a first challenger’s generic in July 2024, 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 Olumiant’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 | |||||
| Tablets, 1 mg and 2 mg | May 2022 | 2 companies | First challenger eligible decided March 2025 | July 2024 | Not yet | June 2030 |
| Tablets, 4 mg | October 2023 | 1 company | First challenger eligible decided August 2025 | August 2025 | Not yet | June 2030 |
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 Baricitinib
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
2 companies have applied to the FDA to make generic baricitinib.
The FDA keeps the other applications private until it acts on them, so those companies are not named here.
First in line. 2 of them were first in line, both 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 Olumiant’s patents with the FDA since May 2022: see the patent challenges.
Approved by the FDA
The FDA has approved generic versions from 1 company, the first in July 2024. Approved is not the same as on sale: patents, a settlement or the company’s own plans can still hold a launch.
For Sale in Pharmacies
Not yet. No company lists a generic baricitinib for sale with the FDA.
| Company | First approved | Strengths | Rated |
|---|---|---|---|
| Msn Laboratories Private Ltd | August 2025 | 1MG, 2MG, 4MG | AB |
| Aurobindo Pharma Ltd discontinued | July 2024 | 1MG, 2MG | – |
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).
Olumiant Price: What Pharmacies Pay and What Generics Usually Do
What Pharmacies Pay for Olumiant 2 mg tablet
$92.54 per tablet in October 2026.
Hover over or tap anywhere on the chart to see that month’s price.
- Olumiant 2 mg tablet $92.54 per tablet
- Olumiant 4 mg tablet $184.66 per tablet
See the numbers
| Month | Pharmacies paid per tablet |
|---|---|
| October 2026 | $92.54 |
| September 2026 | $92.54 |
| August 2026 | $92.53 |
| July 2026 | $92.52 |
| June 2026 | $92.26 |
| May 2026 | $92.29 |
| April 2026 | $92.29 |
| March 2026 | $92.29 |
| February 2026 | $92.29 |
| January 2026 | $92.29 |
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
How we estimate it. We start from what pharmacies pay for Olumiant today: $92.54 per tablet for Olumiant 2 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). Olumiant has 2 companies lined up, so our estimate uses the figure for two companies. More companies would bring the price lower; fewer, less of a drop.
Dollar figures apply FDA’s median drops to the $92.54 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 Olumiant
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 Olumiant, before manufacturer rebates.
- $12.5M
- January to March 2026, the latest CMS has posted
For 1,403 people, about $4,024 per prescription fill - $48.4M
- 2025, the whole year
For 1,909 people, about $3,887 per prescription fill
See the numbers
| Period | Spending | People | Per fill |
|---|---|---|---|
| January to March 2026 | $12,542,690 | 1,403 | $4,023.96 |
| 2025 | $48,350,946 | 1,909 | $3,887.04 |
Source: CMS Medicare Part D Spending by Drug, matched by the brand name Olumiant only, so no generic is counted in it. What CMS says it is used for: Baricitinib is used to treat rheumatoid arthritis. It helps decrease pain, tenderness, and swelling in the joints.
Medicaid Prescriptions by Quarter
5,747 prescriptions in the four quarters to Q1 2026, $26.6M paid.
See the numbers
| Quarter | Prescriptions | Medicaid paid |
|---|---|---|
| Q1 2026 | 630 | $3,835,517 |
| Q4 2025 | 1,664 | $7,619,943 |
| Q3 2025 | 1,804 | $8,048,678 |
| Q2 2025 | 1,649 | $7,139,689 |
| Q1 2025 | 1,487 | $6,470,848 |
Source: CMS Medicaid State Drug Utilization Data, over Olumiant’s own package codes.
Olumiant Strengths and Forms
| Strength | Form | How it is taken | Approved | Status |
|---|---|---|---|---|
| 2MG | Tablet | Oral | May 2018 | Prescription reference product |
| 1MG | Tablet | Oral | October 2019 | Prescription reference product |
| 4MG | Tablet | Oral | May 2022 | Prescription reference product |
Source: FDA Orange Book, Eli Lilly And Co. Listed for sale today by Eli Lilly and Company (FDA NDC Directory).
Olumiant NDC Codes and Packages
Each Olumiant 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 |
|---|---|---|---|
| 00002-4732-30 | BARICITINIB 1 mg/1 tablet, film coated | bottle of 30 tablets | Eli Lilly and Company |
| 00002-4732-30 | BARICITINIB 1 mg/1 tablet, film coated | bottle of 30 tablets | Eli Lilly and Company |
| 00002-4182-30 | BARICITINIB 2 mg/1 tablet, film coated | bottle of 30 tablets | Eli Lilly and Company |
| 00002-4182-30 | BARICITINIB 2 mg/1 tablet, film coated | bottle of 30 tablets | Eli Lilly and Company |
| 00002-4182-61 | BARICITINIB 2 mg/1 tablet, film coated | bottle of 30 tablets | Eli Lilly and Company |
| 00002-4182-61 | BARICITINIB 2 mg/1 tablet, film coated | bottle of 30 tablets | Eli Lilly and Company |
| 00002-4479-30 | BARICITINIB 4 mg/1 tablet, film coated | bottle of 30 tablets | Eli Lilly and Company |
| 00002-4479-30 | BARICITINIB 4 mg/1 tablet, film coated | bottle of 30 tablets | Eli Lilly and Company |
| 00002-4479-61 | BARICITINIB 4 mg/1 tablet, film coated | bottle of 30 tablets | Eli Lilly and Company |
| 00002-4479-61 | BARICITINIB 4 mg/1 tablet, film coated | bottle of 30 tablets | Eli Lilly and Company |
Source: the FDA NDC Directory, current listings only. Only packages sold under Olumiant’s own FDA approval (NDA 207924) are listed, never a generic. Some codes belong to companies that repackage Olumiant: it is the same medicine in a different package.
What a Generic Olumiant Means for You
Nothing Changes Until It Is in Pharmacies
Until a generic is actually for sale, keep filling Olumiant 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 Olumiant”. 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 Olumiant
Is there a generic for Olumiant right now?
No. As of October 9, 2026 no generic baricitinib 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 Olumiant go generic?
January to June 2032 is the expected window, and that is likely 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 November 2032, but it covers a way of using it, not the medicine itself, which a generic can often work around or challenge.
Will generic baricitinib be the same as Olumiant?
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. 2 companies have applied to the FDA to make it. In the FDA’s study of past launches, pharmacies paid about 44% less once two companies sold a generic, which would take the $92.54 pharmacies pay per tablet for Olumiant today to about $51.82. That is a pattern from past launches, not a prediction for this one.
Has the FDA approved a generic Olumiant?
Yes. The FDA Orange Book lists approved generic versions from 1 company, the first approved in July 2024: Msn Laboratories Private Ltd. 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 Olumiant patent expire?
The FDA Orange Book lists 6 patents for Olumiant; the last runs to November 2032. 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 (January to June 2032) weighs all of that.
Has anyone challenged the Olumiant patents?
Yes. The first patent challenge to Olumiant reached the FDA in May 2022, from 2 companies on that first day. The FDA approved a first challenger’s generic in July 2024, 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 Olumiant cost now?
Pharmacies paid about $92.54 per tablet for Olumiant 2 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 January to June 2032 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
- QbrelisLisinoprilDuring 2026
- Triumeq PDAbacavir Sulfate, Dolutegravir Sodium, and LamivudineDuring 2028
- ZepzelcaLurbinectedinDecember 2029
- GenvoyaCobicistat, Elvitegravir, Emtricitabine, and Tenofovir Alafenamide FumarateDuring 2032
- LybalviOlanzapine and Samidorphan L-malateMay 2033
- CaplytaLumateperone TosylateJuly 2040
About Olumiant
- Generic name baricitinib
- How it is taken By mouth
- Company Eli Lilly And Co
- Patent challenges Since May 2022 (FDA)
- More drugs Brand-name drugs starting with O
- Have a question? A pharmacist answers, free. Ask about Olumiant
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.