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Prescription medicine

Erenumab-aooe

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 Erenumab-aooe used for?
The FDA-approved label (Aimovig, Amgen, Inc, July 14, 2026) says: “AIMOVIG is indicated for the preventive treatment of migraine in adults. AIMOVIG is a calcitonin gene-related peptide receptor antagonist indicated for the preventive treatment of migraine in adults.” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Erenumab-aooe have a boxed warning?
No. None of the 1 FDA labels we found for this medicine has a boxed warning.
Is there a shortage of Erenumab-aooe?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Erenumab-aooe been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Erenumab-aooe?
1 company lists prescription products of Erenumab-aooe in the FDA NDC Directory, including Amgen, Inc.

What Erenumab-aooe is used for

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

AIMOVIG is indicated for the preventive treatment of migraine in adults. AIMOVIG is a calcitonin gene-related peptide receptor antagonist indicated for the preventive treatment of migraine in adults.

— FDA label: Aimovig, Amgen, Inc, effective July 14, 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.

Boxed warning

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

The label quoted above has no boxed warning.

Forms and how it is given

Dosage formsInjection · Injection, solution
RouteSubcutaneous
Prescription products4 in the FDA NDC Directory
Brand namesAimovig

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 Erenumab-aooe, by strength and form
Strength and formGeneric or brandPharmacies pay
erenumab 140 mg/mL
injection, solution
Brand: Aimovig $753.27 per mL
erenumab 70 mg/mL
injection
Brand: Aimovig $753.14 per mL

NADAC list of November 4, 2026; these prices took effect on October 21, 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
BLA761077
AIMOVIG
Amgen IncMay 17, 2018 13, latest June 19, 2025
2025: Labeling · 2025: Labeling · 2024: 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)2045627, 2045632, 2045636, 2045638, 2056669, 2056670, 2056680, 2056681, 2120193, 2120195 … (+2)
SPL set ID of the quoted labelb998ed05-94b0-47fd-b28f-cddd1e128fd8
FDA labels (SPL)1
FDA applicationsBLA761077
Active ingredients (FDA)ERENUMAB

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Aimovig, Amgen, Inc, effective July 14, 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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