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Brand-name prescription medicine

Keppra

Generic name: Levetiracetam

FDA application holder: Ucb Inc

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

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 Keppra?
Keppra is a brand name of Levetiracetam, a prescription medicine. The FDA NDC Directory lists 6 Keppra products in 6 strengths and forms.
Who makes Keppra?
Ucb Inc holds the FDA application for Keppra (NDA021035, approved November 30, 1999).
Is there a generic or store brand of Keppra?
Yes. The FDA NDC Directory lists 150 other products with the same active ingredients, strength and form as a Keppra product, 150 of them generic. Ask your pharmacist whether one is right for you.
What do pharmacies pay for Keppra?
CMS lists a National Average Drug Acquisition Cost (NADAC) for 5 Keppra strengths and forms (see the table below). That is what pharmacies pay to buy it, not what you pay: your price depends on your insurance and your pharmacy.
Has Keppra been recalled?
FDA enforcement reports list 1 recall of Keppra products; the newest started July 18, 2019. A recall usually concerns specific lots, not every product.

What Keppra is

Each Keppra product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Levetiracetam · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
levetiracetam 100 mg/mL
injection, solution, concentrate (intravenous)
Keppra 4 products, 4 companies DailyMed
levetiracetam 100 mg/mL
solution (oral)
Keppra 25 products, 22 companies DailyMed
levetiracetam 1000 mg
tablet, film coated (oral)
Keppra 29 products, 22 companies DailyMed
levetiracetam 250 mg
tablet, film coated (oral)
Keppra 26 products, 24 companies DailyMed
levetiracetam 500 mg
tablet, film coated (oral)
Keppra 42 products, 33 companies DailyMed
levetiracetam 750 mg
tablet, film coated (oral)
Keppra 24 products, 22 companies DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Levetiracetam →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Keppra products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA021035Ucb IncNovember 30, 19994
NDA021505Ucb IncJuly 15, 20031
NDA021872Ucb IncJuly 31, 20061

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 Keppra, by strength and form
Strength and formGeneric or brandPharmacies pay
levetiracetam 100 mg/mL
solution
Brand: Keppra $1.92 per mL
Generic of the same strength and form: $0.0299 per mL
levetiracetam 1000 mg
tablet, film coated
Brand: Keppra $19.87 per tablet
Generic of the same strength and form: $0.1645 per tablet
levetiracetam 250 mg
tablet, film coated
Brand: Keppra $8.08 per tablet
Generic of the same strength and form: $0.0568 per tablet
levetiracetam 500 mg
tablet, film coated
Brand: Keppra $9.92 per tablet
Generic of the same strength and form: $0.0722 per tablet
levetiracetam 750 mg
tablet, film coated
Brand: Keppra $13.45 per tablet
Generic of the same strength and form: $0.1107 per tablet

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 Keppra

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Keppra products.

Recalls

From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific lots: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.

  1. July 18, 2019 · Class II · Terminated · D-1838-2019

    Failed Dissolution Specifications.

    Keppra (levetiracetam) 1000 mg tablets, 60 tablets per bottle, Rx only, Manufactured for UCB, Inc. Smyrna, GA 30080, NDC 50474-597-66. — Ucb, Inc

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, 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. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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