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Prescription medicine

Etanercept

Drug class: Tumor Necrosis Factor Blocker

The FDA’s “Established Pharmacologic Class”: the group of medicines that work in a similar way.

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Etanercept used for?
The FDA-approved label (Enbrel, Immunex Corporation, May 11, 2026) says: “Enbrel is a tumor necrosis factor (TNF) blocker indicated for the treatment of: Adult patients with: Rheumatoid Arthritis (RA) Psoriatic Arthritis (PsA) Ankylosing Spondylitis (AS) Plaque Psoriasis (PsO) Pediatric patients with …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Etanercept have a boxed warning?
Yes. The FDA label for Enbrel has a boxed warning, the FDA’s strongest warning. Read it on the full label and ask your pharmacist.
Is there a shortage of Etanercept?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Etanercept been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Etanercept?
1 company lists prescription products of Etanercept in the FDA NDC Directory, including Immunex Corporation.

What Etanercept is used for

Quoted from the “Indications and Usage” section of the FDA-approved label.

Enbrel is a tumor necrosis factor (TNF) blocker indicated for the treatment of: Adult patients with: Rheumatoid Arthritis (RA) Psoriatic Arthritis (PsA) Ankylosing Spondylitis (AS) Plaque Psoriasis (PsO) Pediatric patients with …

— FDA label: Enbrel, Immunex Corporation, effective May 11, 2026. Read the full label on DailyMed →

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

Conditions named on the label

These condition names appear word for word in the label’s “Indications and Usage” text (matched with a reviewed table). Each page lists hospitals whose own websites name the condition.

Related medical specialties

Boxed warning

A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.

This label has a boxed warning. Read it on the full label →

Forms and how it is given

Dosage formsSolution
RouteSubcutaneous
Prescription products5 in the FDA NDC Directory
Brand namesEnbrel

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Etanercept, by strength and form
Strength and formGeneric or brandPharmacies pay
etanercept 25 mg/0.5 mL
solution
Brand: Enbrel $2,083.78 per mL
etanercept 50 mg/mL
solution
Brand: Enbrel $2,080.97–$2,083.62 per mL
4 packages, lowest to highest

NADAC list of November 4, 2026; these prices took effect between October 21, 2026 and October 28, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

Companies that list this medicine

Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.

FDA approval history

  • BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
Brand and biologic applications
ApplicationSponsorApprovedLater changes approved
BLA103795
ENBREL
ImmunexNovember 2, 1998 94, latest October 14, 2026
2026: Labeling · 2026: Labeling · 2025: Labeling

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.

Official identifiers

RxCUI (RxNorm)253014, 261105, 727757, 802652, 809158, 809159, 1653223, 1653225, 2182338, 2182340 … (+2)
SPL set ID of the quoted labela002b40c-097d-47a5-957f-7a7b1807af7f
FDA labels (SPL)1
FDA applicationsBLA103795
Active ingredients (FDA)ETANERCEPT

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Enbrel, Immunex Corporation, effective May 11, 2026; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026

openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →

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