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Prescription medicine

Adalimumab-aaty Brand names: Yuflyma

Adalimumab-aaty (Yuflyma) is a prescription medicine with an FDA approval on record since 2023. No generic is listed; pharmacies paid $495.75 per unit (Adalimumab-aaty(cf) 40 mg/0.4 mL autoinjector) in the October 7, 2026 NADAC survey.

  • No generic listed
  • Boxed warning

Check it at the source: the adalimumab-aaty FDA label on DailyMed (effective July 8, 2026, CELLTRION USA, Inc.); the BLA 761219 record on Drugs@FDA; every adalimumab-aaty label on DailyMed.

Highlights of the record

FDA label of July 8, 2026; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026; NADAC October 7, 2026

Boxed warning

SERIOUS INFECTIONS and MALIGNANCY WARNING: SERIOUS INFECTIONS and MALIGNANCY See full prescribing information for complete boxed warning. SERIOUS INFECTIONS ( 5.1 , 6.1 ): Increased risk of serious infections leading to hospitalization or death, including tuberculosis (TB), bacterial sepsis, invasive fungal infections (such as histoplasmosis), and infections due to other opportunistic pathogens. Discontinue Adalimumab-aaty if a patient develops a serious infection or sepsis during treatment. Perform test for latent TB; if positive, start treatment for TB prior to starting Adalimumab-aaty. Monitor all patients for active TB during treatment, even if initial latent TB test is negative. MALIGNANCY ( 5.2 ): Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with TNF blockers including adalimumab products. Post-marketing cases of hepatosplenic T-cell lymphoma (HSTCL), a rare type of T-cell lymphoma, have occurred in adolescent and young adults with inflammatory bowel disease treated with TNF blockers including adalimumab products. SERIOUS INFECTIONS Patients treated with adalimumab products, including Adalimumab-aaty, are at increased risk for developing serious infections that may lead to hospitalization or death [see Warnings and Precautions ( 5.1 )]. […]

Used for

From the label: indications and usage

Adalimumab-aaty is a tumor necrosis factor (TNF) blocker indicated for: Reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage, and improving physical function in adult patients with moderately to severely active r heumatoid arthritis.

Forms and strengths

Kit.

On the market

Earliest approval on file
May 23, 2023 Yuflyma, Celltrion; Drugs@FDA’s file, where older or withdrawn approvals can be missing
Generic approvals
No generic approved
Labelers listed (NDC)
1 of which 0 under generic applications, 1 under brand applications, repackagers included

Supply and safety

Pharmacy cost (NADAC)
$495.75 per unit Adalimumab-aaty(cf) 40 mg/0.4 mL autoinjector
Shortage (FDA)
No current entry
Recalls by its makers (FDA)
No recall recorded
FAERS reports
47,055 through July 30, 2026

What is adalimumab-aaty used for?

From the label: indications and usage

Adalimumab-aaty is a tumor necrosis factor (TNF) blocker indicated for: Reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage, and improving physical function in adult patients with moderately to severely active r heumatoid arthritis. ( 1.1 ) Reducing signs and symptoms of moderately to severely active polyarticular juvenile idiopathic arthritis in patients 2 years of age and older. ( 1.2 ) Reducing signs and symptoms, inhibiting the progression of structural damage, and improving physical function in adult patients with active p soriatic arthritis. […]

Conditions named in the indications of adalimumab-aaty's FDA labels, with every medicine labeled for each:

From other adalimumab-aaty labels

Psoriasis: Treatment of adult patients with moderate to severe chronic plaque psoriasis who are candidates for systemic therapy or phototherapy, and when other systemic therapies are medically less appropriate. …

Rheumatoid arthritis: Rheumatoid Arthritis Adalimumab-aaty is indicated for reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage, and improving physical function in adult patients with moderately to …

Crohn's disease and ulcerative colitis: Crohn's Disease Adalimumab-aaty is indicated for the treatment of moderately to severely active Crohn's disease in adults and pediatric patients 6 years of age and older.

Source: FDA drug label (Adalimumab), CELLTRION USA, Inc., effective July 8, 2026 (SPL set c44365e9-d470-4e35-978d-8565a9e3471e), via openFDA; the full label on DailyMed

What does the patient leaflet for adalimumab-aaty say first?

The FDA-approved Medication Guide or Patient Information that comes with the medicine, in its own words.

From the patient leaflet: What is the most important information I should know about Adalimumab-aaty?

Adalimumab-aaty is a medicine that affects your immune system. Adalimumab-aaty can lower the ability of your immune system to fight infections. Serious infections have happened in people taking adalimumab products. These serious infections include tuberculosis (TB) and infections caused by viruses, fungi or bacteria that have spread throughout the body. Some people have died from these infections. Your doctor should test you for TB before starting Adalimumab-aaty. Your doctor should check you closely for signs and symptoms of TB during treatment with Adalimumab-aaty. You should not start taking Adalimumab-aaty if you have any kind of infection unless your doctor says it is okay. Before starting Adalimumab-aaty, tell your doctor if you: think you have an infection or have symptoms of infection such as: fever, sweats, or chills muscle aches cough shortness of breath blood in phlegm warm, red, or painful skin or sores on your body diarrhea or stomach pain burning when you urinate or urinate more often than normal feel very tired weight loss are being treated for an infection. get a lot of infections or have infections that keep coming back. have diabetes. have TB, or have been in close contact with someone with TB. were born in, lived in, or traveled to countries where there is more risk for getting TB. Ask your doctor if you are not sure. live or have lived in certain parts of the country (such as the Ohio and Mississippi River valleys) where there is an increased risk for getting certain kinds of fungal infections (histoplasmosis, coccidioidomycosis, or blastomycosis). These infections may happen or become more severe if you use Adalimumab-aaty. […]

From the patient leaflet: How should I store Adalimumab-aaty?

Store Adalimumab-aaty in the refrigerator at 36°F to 46°F (2°C to 8°C). Store Adalimumab-aaty in the original carton until use to protect it from light. Do not shake. Do not freeze Adalimumab-aaty. Do not use Adalimumab-aaty if frozen, even if it has been thawed. Refrigerated Adalimumab-aaty may be used until the expiration date printed on the Adalimumab-aaty carton, dose pack, auto-injector or prefilled syringe. Do not use Adalimumab-aaty after the expiration date. If needed, for example when you are traveling, you may also store Adalimumab-aaty at room temperature up to 77°F (25°C) for up to 31 days. Store Adalimumab-aaty in the original carton until use to protect it from light. Throw away Adalimumab-aaty if it has been kept at room temperature and not been used within 31 days. […]

Source: FDA drug label (Adalimumab), CELLTRION USA, Inc., effective July 8, 2026 (SPL set c44365e9-d470-4e35-978d-8565a9e3471e), via openFDA; the full label on DailyMed

Is there a generic for adalimumab-aaty (Yuflyma)?

No generic adalimumab-aaty is approved (Drugs@FDA, October 8, 2026).

  • 2023 earliest approval on file

Source: Drugs@FDA, FDA NDC Directory and the Orange Book (openFDA bulk files, October 8, 2026)

What do pharmacies pay for adalimumab-aaty (Yuflyma)?

In CMS's NADAC survey of October 7, 2026, pharmacies paid $495.75 per unit (Adalimumab-aaty(cf) 40 mg/0.4 mL autoinjector). The chart's scale runs from the lowest to the highest price shown, not from zero. NADAC is what retail pharmacies paid their wholesalers, per unit, in CMS's monthly survey; what a patient pays depends on insurance and the pharmacy.

  • Adalimumab-aaty(cf) 40 mg/0.4 mL autoinjector (generic)
  • Yuflyma(cf) 40 mg/0.4 mL autoinjector (brand)
$912.38
$493.15
February 2026October 2026
NADAC per unit, October 7, 2026
Strength and formBrand or genericPharmacy cost30 tablets, or one pen or vial12-month change
Adalimumab-aaty(cf) 40 mg/0.4 mL autoinjectorGeneric$495.75 per unitn/an/a
Yuflyma(cf) 40 mg/0.4 mL autoinjectorBrand$904.53 per unitn/an/a

Source: CMS National Average Drug Acquisition Cost (NADAC) survey, October 7, 2026: what retail pharmacies paid per unit; not a counter price

What does the adalimumab-aaty label say about other medicines?

The adalimumab-aaty label names 9 other medicines in its interaction, contraindication or warning sections. The sentences are the labels' own; a label lists what its studies and reports found, not every interaction.

Medicine namedSectionWhat the label says
Abataceptdrug interactionsDRUG INTERACTIONS Abatacept: Increased risk of serious infection ( 5.1 , 5.11 , 7.2 ) Anakinra:
Adalimumabboxed warningSERIOUS INFECTIONS Patients treated with adalimumab products, including Adalimumab-aaty, are at increased risk for developing serious infections that may lead to hospitalization or death [see Warnings and Precautions ( 5.1 )].
Anakinradrug interactionsDRUG INTERACTIONS Abatacept: Increased risk of serious infection ( 5.1 , 5.11 , 7.2 ) Anakinra:
Azathioprineboxed warningAlmost all these patients had received treatment with azathioprine or 6-mercaptopurine (6–MP) concomitantly with a TNF blocker at or prior to diagnosis.
Cyclosporinedrug interactionsUpon initiation or discontinuation of Adalimumab-aaty in patients being treated with CYP450 substrates with a narrow therapeutic index, monitoring of the effect (e.g., warfarin) or drug concentration (e.g., cyclosporine or theophylline) is recommended and the individual dose of the drug product may be adjusted as …
Methotrexateboxed warningMost patients who developed these infections were taking concomitant immunosuppressants such as methotrexate or corticosteroids.
Rituximabdrug interactionsA higher rate of serious infections has also been observed in patients with RA treated with rituximab who received subsequent treatment with a TNF blocker.
Theophyllinedrug interactionsUpon initiation or discontinuation of Adalimumab-aaty in patients being treated with CYP450 substrates with a narrow therapeutic index, monitoring of the effect (e.g., warfarin) or drug concentration (e.g., cyclosporine or theophylline) is recommended and the individual dose of the drug product may be adjusted as …
Warfarindrug interactionsUpon initiation or discontinuation of Adalimumab-aaty in patients being treated with CYP450 substrates with a narrow therapeutic index, monitoring of the effect (e.g., warfarin) or drug concentration (e.g., cyclosporine or theophylline) is recommended and the individual dose of the drug product may be adjusted as …

Check adalimumab-aaty against other medicines

Source: FDA drug label (Adalimumab), CELLTRION USA, Inc., effective July 8, 2026 (SPL set c44365e9-d470-4e35-978d-8565a9e3471e), via openFDA; the full label on DailyMed

What do FAERS reports show for adalimumab-aaty?

The FDA Adverse Event Reporting System holds 47,055 reports that list adalimumab-aaty among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 6,925 are coded as a death and 16,264 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is. Reports rose sharply in 2025 (9,558, against a median of 2,715 a year): FAERS counts follow reporting, which news, litigation and label changes can drive, not how often a reaction happens.

Reports received each year

The most reported reactions

  • Drug Ineffective (a use or a product term, not a reaction)10,565
  • Off Label Use (a use or a product term, not a reaction)8,305
  • Rheumatoid Arthritis (a use or a product term, not a reaction)5,745
  • Fatigue5,525
  • Pain5,471
  • Arthralgia (named in the label)5,250
  • Rash (named in the label)4,668
  • Condition Aggravated (a use or a product term, not a reaction)4,531

Side effects: the label's list and every FAERS reaction

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026

What next?

Adalimumab-aaty side effects
the label's list beside FAERS reports
Check an interaction
what two or more labels say about each other