United States · FDA National Drug Code directory
Levetiracetam ER
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 69367-333_18d684d2-22a4-497a-ab10-f35ef53408ce
- Product NDC
- 69367-333
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Levetiracetam
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210930
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVETIRACETAM — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69367-333-60) · 69367-333-60
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →