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Brand-name prescription medicine

Elepsia XR 1000 Mg

Generic name: Levetiracetam

FDA application holder: Tripoint

Strengths and generic versions Official label

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.

At a glance

1Strengths and forms
0Same medicine, other names
2018FDA approval
0Recalls (FDA reports)

Quick answers

What is Elepsia XR 1000 Mg?
Elepsia XR 1000 Mg is a brand name of Levetiracetam, a prescription medicine. The FDA NDC Directory lists 1 Elepsia XR 1000 Mg product in 1 strength and form.
Who makes Elepsia XR 1000 Mg?
Tripoint holds the FDA application for Elepsia XR 1000 Mg (NDA204417, approved December 20, 2018).
Is there a generic or store brand of Elepsia XR 1000 Mg?
Other products of Levetiracetam are listed with the FDA, but none in exactly the same strength and form as a Elepsia XR 1000 Mg product.
Has Elepsia XR 1000 Mg been recalled?
No recall linked to Elepsia XR 1000 Mg products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Elepsia XR 1000 Mg is

Each Elepsia XR 1000 Mg 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 1000 mg
tablet, extended release (oral)		 Elepsia XR 1000 Mg None listed 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 Elepsia XR 1000 Mg products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA204417TripointDecember 20, 20181

Companies that list Elepsia XR 1000 Mg

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Elepsia XR 1000 Mg products.

Recalls

No recall linked to Elepsia XR 1000 Mg products (by their NDC code or label) appears in the FDA enforcement reports.

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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